Canonical Allele Identifier: CA1144663403
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914873C= , CM000663.2:g.173914873C= GRCh38
NC_000001.10:g.173884011C= , CM000663.1:g.173884011C= GRCh37
NC_000001.9:g.172150634C= NCBI36
NG_012462.1:g.7506G= , LRG_577:g.7506G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.88G= MANE Select ENSP00000356671.3:p.Val30=
ENST00000367698.3:c.88G= ENSP00000356671.3:p.Val30=
ENST00000494024.1:n.314G=
ENST00000617423.4:c.88G= ENSP00000478688.1:p.Val30=
NM_000488.3:c.88G= , LRG_577t1:c.88G= NP_000479.1:p.Val30=
XM_005245198.2:c.-57G= XP_005245255.1:n.-57G=
NM_001365052.1:c.-57G= NP_001351981.1:n.-57G=
NM_000488.4:c.88G= MANE Select NP_000479.1:p.Val30=
NM_001365052.2:c.-57G= NP_001351981.1:n.-57G=
NM_001386302.1:c.88G= NP_001373231.1:p.Val30=
NM_001386303.1:c.169G= NP_001373232.1:p.Val57=
NM_001386304.1:c.88G= NP_001373233.1:p.Val30=
NM_001386305.1:c.88G= NP_001373234.1:p.Val30=
NM_001386306.1:c.88G= NP_001373235.1:p.Val30=