Canonical Allele Identifier: CA1607966655

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6167516C= , CM000668.2:g.6167516C=	GRCh38
NC_000006.11:g.6167749C= , CM000668.1:g.6167749C=	GRCh37
NC_000006.10:g.6112748C=	NCBI36
NG_008107.1:g.158176G= , LRG_549:g.158176G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.1850G= MANE Select	ENSP00000264870.3:p.Arg617=
ENST00000264870.7:c.1850G=	ENSP00000264870.3:p.Arg617=
NM_000129.3:c.1850G= , LRG_549t1:c.1850G=	NP_000120.2:p.Arg617=
XM_006715010.2:c.1850G=	XP_006715073.1:p.Arg617=
XM_011514342.1:c.2012G=	XP_011512644.1:p.Arg671=
NM_000129.4:c.1850G= MANE Select	NP_000120.2:p.Arg617=