Canonical Allele Identifier: CA2649174160
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904146_173904147insTTTGAGGA , CM000663.2:g.173904146_173904147insTTTGAGGA GRCh38
NC_000001.10:g.173873284_173873285insTTTGAGGA , CM000663.1:g.173873284_173873285insTTTGAGGA GRCh37
NC_000001.9:g.172139907_172139908insTTTGAGGA NCBI36
NG_012462.1:g.18233_18234insCCTCAAAT , LRG_577:g.18233_18234insCCTCAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-81_1219-80insCCTCAAAT MANE Select ENSP00000356671.3:n.1219-81_1219-80insCCTCAAAT
ENST00000367698.3:c.1219-81_1219-80insCCTCAAAT ENSP00000356671.3:n.1219-81_1219-80insCCTCAAAT
ENST00000617423.4:c.604-81_604-80insCCTCAAAT ENSP00000478688.1:n.604-81_604-80insCCTCAAAT
NM_000488.3:c.1219-81_1219-80insCCTCAAAT , LRG_577t1:c.1219-81_1219-80insCCTCAAAT NP_000479.1:n.1219-81_1219-80insCCTCAAAT
XM_005245198.2:c.1075-81_1075-80insCCTCAAAT XP_005245255.1:n.1075-81_1075-80insCCTCAAAT
NM_001365052.1:c.1075-81_1075-80insCCTCAAAT NP_001351981.1:n.1075-81_1075-80insCCTCAAAT
NM_000488.4:c.1219-81_1219-80insCCTCAAAT MANE Select NP_000479.1:n.1219-81_1219-80insCCTCAAAT
NM_001365052.2:c.1075-81_1075-80insCCTCAAAT NP_001351981.1:n.1075-81_1075-80insCCTCAAAT
NM_001386302.1:c.1342-81_1342-80insCCTCAAAT NP_001373231.1:n.1342-81_1342-80insCCTCAAAT
NM_001386303.1:c.1300-81_1300-80insCCTCAAAT NP_001373232.1:n.1300-81_1300-80insCCTCAAAT
NM_001386304.1:c.1198-81_1198-80insCCTCAAAT NP_001373233.1:n.1198-81_1198-80insCCTCAAAT
NM_001386305.1:c.1162-81_1162-80insCCTCAAAT NP_001373234.1:n.1162-81_1162-80insCCTCAAAT
NM_001386306.1:c.1003-81_1003-80insCCTCAAAT NP_001373235.1:n.1003-81_1003-80insCCTCAAAT