Canonical Allele Identifier: CA1207934367
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903927T= , CM000663.2:g.173903927T= GRCh38
NC_000001.10:g.173873065T= , CM000663.1:g.173873065T= GRCh37
NC_000001.9:g.172139688T= NCBI36
NG_012462.1:g.18452A= , LRG_577:g.18452A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1357A= MANE Select ENSP00000356671.3:p.Ile453=
ENST00000367698.3:c.1357A= ENSP00000356671.3:p.Ile453=
ENST00000617423.4:c.742A= ENSP00000478688.1:p.Ile248=
NM_000488.3:c.1357A= , LRG_577t1:c.1357A= NP_000479.1:p.Ile453=
XM_005245198.2:c.1213A= XP_005245255.1:p.Ile405=
NM_001365052.1:c.1213A= NP_001351981.1:p.Ile405=
NM_000488.4:c.1357A= MANE Select NP_000479.1:p.Ile453=
NM_001365052.2:c.1213A= NP_001351981.1:p.Ile405=
NM_001386302.1:c.1480A= NP_001373231.1:p.Ile494=
NM_001386303.1:c.1438A= NP_001373232.1:p.Ile480=
NM_001386304.1:c.1336A= NP_001373233.1:p.Ile446=
NM_001386305.1:c.1300A= NP_001373234.1:p.Ile434=
NM_001386306.1:c.1141A= NP_001373235.1:p.Ile381=