Canonical Allele Identifier: CA1207936905
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909599T= , CM000663.2:g.173909599T= GRCh38
NC_000001.10:g.173878737T= , CM000663.1:g.173878737T= GRCh37
NC_000001.9:g.172145360T= NCBI36
NG_012462.1:g.12780A= , LRG_577:g.12780A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1106A= MANE Select ENSP00000356671.3:p.Asp369=
ENST00000367698.3:c.1106A= ENSP00000356671.3:p.Asp369=
ENST00000617423.4:c.560-2106A= ENSP00000478688.1:n.560-2106A=
NM_000488.3:c.1106A= , LRG_577t1:c.1106A= NP_000479.1:p.Asp369=
XM_005245198.2:c.962A= XP_005245255.1:p.Asp321=
NM_001365052.1:c.962A= NP_001351981.1:p.Asp321=
NM_000488.4:c.1106A= MANE Select NP_000479.1:p.Asp369=
NM_001365052.2:c.962A= NP_001351981.1:p.Asp321=
NM_001386302.1:c.1229A= NP_001373231.1:p.Asp410=
NM_001386303.1:c.1187A= NP_001373232.1:p.Asp396=
NM_001386304.1:c.1085A= NP_001373233.1:p.Asp362=
NM_001386305.1:c.1049A= NP_001373234.1:p.Asp350=
NM_001386306.1:c.890A= NP_001373235.1:p.Asp297=