Canonical Allele Identifier: CA1608002839

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6248364T= , CM000668.2:g.6248364T=	GRCh38
NC_000006.11:g.6248597T= , CM000668.1:g.6248597T=	GRCh37
NC_000006.10:g.6193596T=	NCBI36
NG_008107.1:g.77328A= , LRG_549:g.77328A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.746A= MANE Select	ENSP00000264870.3:p.Asp249=
ENST00000264870.7:c.746A=	ENSP00000264870.3:p.Asp249=
NM_000129.3:c.746A= , LRG_549t1:c.746A=	NP_000120.2:p.Asp249=
XM_006715010.2:c.746A=	XP_006715073.1:p.Asp249=
XM_011514342.1:c.908A=	XP_011512644.1:p.Asp303=
NM_000129.4:c.746A= MANE Select	NP_000120.2:p.Asp249=