Canonical Allele Identifier: CA1607973390

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182028A= , CM000668.2:g.6182028A=	GRCh38
NC_000006.11:g.6182261A= , CM000668.1:g.6182261A=	GRCh37
NC_000006.10:g.6127260A=	NCBI36
NG_008107.1:g.143664T= , LRG_549:g.143664T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.1419T= MANE Select	ENSP00000264870.3:p.Asp473=
ENST00000264870.7:c.1419T=	ENSP00000264870.3:p.Asp473=
NM_000129.3:c.1419T= , LRG_549t1:c.1419T=	NP_000120.2:p.Asp473=
XM_006715010.2:c.1419T=	XP_006715073.1:p.Asp473=
XM_011514342.1:c.1581T=	XP_011512644.1:p.Asp527=
NM_000129.4:c.1419T= MANE Select	NP_000120.2:p.Asp473=