Canonical Allele Identifier: CA2586967707
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903989_173903990insGA , CM000663.2:g.173903989_173903990insGA GRCh38
NC_000001.10:g.173873127_173873128insGA , CM000663.1:g.173873127_173873128insGA GRCh37
NC_000001.9:g.172139750_172139751insGA NCBI36
NG_012462.1:g.18390_18391insCT , LRG_577:g.18390_18391insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1295_1296insCT MANE Select ENSP00000356671.3:p.Thr433Ter
ENST00000367698.3:c.1295_1296insCT ENSP00000356671.3:p.Thr433Ter
ENST00000617423.4:c.680_681insCT ENSP00000478688.1:p.Thr228Ter
NM_000488.3:c.1295_1296insCT , LRG_577t1:c.1295_1296insCT NP_000479.1:p.Thr433Ter
XM_005245198.2:c.1151_1152insCT XP_005245255.1:p.Thr385Ter
NM_001365052.1:c.1151_1152insCT NP_001351981.1:p.Thr385Ter
NM_000488.4:c.1295_1296insCT MANE Select NP_000479.1:p.Thr433Ter
NM_001365052.2:c.1151_1152insCT NP_001351981.1:p.Thr385Ter
NM_001386302.1:c.1418_1419insCT NP_001373231.1:p.Thr474Ter
NM_001386303.1:c.1376_1377insCT NP_001373232.1:p.Thr460Ter
NM_001386304.1:c.1274_1275insCT NP_001373233.1:p.Thr426Ter
NM_001386305.1:c.1238_1239insCT NP_001373234.1:p.Thr414Ter
NM_001386306.1:c.1079_1080insCT NP_001373235.1:p.Thr361Ter
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