Canonical Allele Identifier: CA2586967696
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903894dup , CM000663.2:g.173903894dup GRCh38
NC_000001.10:g.173873032dup , CM000663.1:g.173873032dup GRCh37
NC_000001.9:g.172139655dup NCBI36
NG_012462.1:g.18486dup , LRG_577:g.18486dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1391dup MANE Select ENSP00000356671.3:p.Ter465ValextTer19
ENST00000367698.3:c.1391dup ENSP00000356671.3:p.Ter465ValextTer19
ENST00000617423.4:c.776dup ENSP00000478688.1:p.Ter260ValextTer19
NM_000488.3:c.1391dup , LRG_577t1:c.1391dup NP_000479.1:p.Ter465ValextTer19
XM_005245198.2:c.1247dup XP_005245255.1:p.Ter417ValextTer19
NM_001365052.1:c.1247dup NP_001351981.1:p.Ter417ValextTer19
NM_000488.4:c.1391dup MANE Select NP_000479.1:p.Ter465ValextTer19
NM_001365052.2:c.1247dup NP_001351981.1:p.Ter417ValextTer19
NM_001386302.1:c.1514dup NP_001373231.1:p.Ter506ValextTer19
NM_001386303.1:c.1472dup NP_001373232.1:p.Ter492ValextTer19
NM_001386304.1:c.1370dup NP_001373233.1:p.Ter458ValextTer19
NM_001386305.1:c.1334dup NP_001373234.1:p.Ter446ValextTer19
NM_001386306.1:c.1175dup NP_001373235.1:p.Ter393ValextTer19
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