Canonical Allele Identifier: CA2697768480
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs2102773029

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903947_173903949dup , CM000663.2:g.173903947_173903949dup GRCh38
NC_000001.10:g.173873085_173873087dup , CM000663.1:g.173873085_173873087dup GRCh37
NC_000001.9:g.172139708_172139710dup NCBI36
NG_012462.1:g.18432_18434dup , LRG_577:g.18432_18434dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1337_1339dup MANE Select ENSP00000356671.3:p.Glu446_Val447insGlu
ENST00000367698.3:c.1337_1339dup ENSP00000356671.3:p.Glu446_Val447insGlu
ENST00000617423.4:c.722_724dup ENSP00000478688.1:p.Glu241_Val242insGlu
NM_000488.3:c.1337_1339dup , LRG_577t1:c.1337_1339dup NP_000479.1:p.Glu446_Val447insGlu
XM_005245198.2:c.1193_1195dup XP_005245255.1:p.Glu398_Val399insGlu
NM_001365052.1:c.1193_1195dup NP_001351981.1:p.Glu398_Val399insGlu
NM_000488.4:c.1337_1339dup MANE Select NP_000479.1:p.Glu446_Val447insGlu
NM_001365052.2:c.1193_1195dup NP_001351981.1:p.Glu398_Val399insGlu
NM_001386302.1:c.1460_1462dup NP_001373231.1:p.Glu487_Val488insGlu
NM_001386303.1:c.1418_1420dup NP_001373232.1:p.Glu473_Val474insGlu
NM_001386304.1:c.1316_1318dup NP_001373233.1:p.Glu439_Val440insGlu
NM_001386305.1:c.1280_1282dup NP_001373234.1:p.Glu427_Val428insGlu
NM_001386306.1:c.1121_1123dup NP_001373235.1:p.Glu374_Val375insGlu