Canonical Allele Identifier: CA343774004
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909725A>C , CM000663.2:g.173909725A>C GRCh38
NC_000001.10:g.173878863A>C , CM000663.1:g.173878863A>C GRCh37
NC_000001.9:g.172145486A>C NCBI36
NG_012462.1:g.12654T>G , LRG_577:g.12654T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.980T>G MANE Select ENSP00000356671.3:p.Val327Gly
ENST00000367698.3:c.980T>G ENSP00000356671.3:p.Val327Gly
ENST00000617423.4:c.559+2139T>G ENSP00000478688.1:n.559+2139T>G
NM_000488.3:c.980T>G , LRG_577t1:c.980T>G NP_000479.1:p.Val327Gly
XM_005245198.2:c.836T>G XP_005245255.1:p.Val279Gly
NM_001365052.1:c.836T>G NP_001351981.1:p.Val279Gly
NM_000488.4:c.980T>G MANE Select NP_000479.1:p.Val327Gly
NM_001365052.2:c.836T>G NP_001351981.1:p.Val279Gly
NM_001386302.1:c.1103T>G NP_001373231.1:p.Val368Gly
NM_001386303.1:c.1061T>G NP_001373232.1:p.Val354Gly
NM_001386304.1:c.959T>G NP_001373233.1:p.Val320Gly
NM_001386305.1:c.923T>G NP_001373234.1:p.Val308Gly
NM_001386306.1:c.764T>G NP_001373235.1:p.Val255Gly