Canonical Allele Identifier: CA1207937823

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911900C= , CM000663.2:g.173911900C=	GRCh38
NC_000001.10:g.173881038C= , CM000663.1:g.173881038C=	GRCh37
NC_000001.9:g.172147661C=	NCBI36
NG_012462.1:g.10479G= , LRG_577:g.10479G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.523G= MANE Select	ENSP00000356671.3:p.Ala175=
ENST00000367698.3:c.523G=	ENSP00000356671.3:p.Ala175=
ENST00000487183.1:n.228G=
ENST00000617423.4:c.523G=	ENSP00000478688.1:p.Ala175=
NM_000488.3:c.523G= , LRG_577t1:c.523G=	NP_000479.1:p.Ala175=
XM_005245198.2:c.379G=	XP_005245255.1:p.Ala127=
NM_001365052.1:c.379G=	NP_001351981.1:p.Ala127=
NM_000488.4:c.523G= MANE Select	NP_000479.1:p.Ala175=
NM_001365052.2:c.379G=	NP_001351981.1:p.Ala127=
NM_001386302.1:c.523G=	NP_001373231.1:p.Ala175=
NM_001386303.1:c.604G=	NP_001373232.1:p.Ala202=
NM_001386304.1:c.523G=	NP_001373233.1:p.Ala175=
NM_001386305.1:c.523G=	NP_001373234.1:p.Ala175=
NM_001386306.1:c.409-1009G=	NP_001373235.1:n.409-1009G=