Canonical Allele Identifier: CA1607973416

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182102C= , CM000668.2:g.6182102C=	GRCh38
NC_000006.11:g.6182335C= , CM000668.1:g.6182335C=	GRCh37
NC_000006.10:g.6127334C=	NCBI36
NG_008107.1:g.143590G= , LRG_549:g.143590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1345G= MANE Select	ENSP00000264870.3:p.Gly449=
ENST00000264870.7:c.1345G=	ENSP00000264870.3:p.Gly449=
NM_000129.3:c.1345G= , LRG_549t1:c.1345G=	NP_000120.2:p.Gly449=
XM_006715010.2:c.1345G=	XP_006715073.1:p.Gly449=
XM_011514342.1:c.1507G=	XP_011512644.1:p.Gly503=
NM_000129.4:c.1345G= MANE Select	NP_000120.2:p.Gly449=