Canonical Allele Identifier: CA1142368681

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909795A= , CM000663.2:g.173909795A=	GRCh38
NC_000001.10:g.173878933A= , CM000663.1:g.173878933A=	GRCh37
NC_000001.9:g.172145556A=	NCBI36
NG_012462.1:g.12584T= , LRG_577:g.12584T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.910T= MANE Select	ENSP00000356671.3:p.Leu304=
ENST00000367698.3:c.910T=	ENSP00000356671.3:p.Leu304=
ENST00000487183.1:n.561T=
ENST00000617423.4:c.559+2069T=	ENSP00000478688.1:n.559+2069T=
NM_000488.3:c.910T= , LRG_577t1:c.910T=	NP_000479.1:p.Leu304=
XM_005245198.2:c.766T=	XP_005245255.1:p.Leu256=
NM_001365052.1:c.766T=	NP_001351981.1:p.Leu256=
NM_000488.4:c.910T= MANE Select	NP_000479.1:p.Leu304=
NM_001365052.2:c.766T=	NP_001351981.1:p.Leu256=
NM_001386302.1:c.1033T=	NP_001373231.1:p.Leu345=
NM_001386303.1:c.991T=	NP_001373232.1:p.Leu331=
NM_001386304.1:c.889T=	NP_001373233.1:p.Leu297=
NM_001386305.1:c.853T=	NP_001373234.1:p.Leu285=
NM_001386306.1:c.694T=	NP_001373235.1:p.Leu232=