Canonical Allele Identifier: CA1607973425

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182132C= , CM000668.2:g.6182132C=	GRCh38
NC_000006.11:g.6182365C= , CM000668.1:g.6182365C=	GRCh37
NC_000006.10:g.6127364C=	NCBI36
NG_008107.1:g.143560G= , LRG_549:g.143560G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1315G= MANE Select	ENSP00000264870.3:p.Asp439=
ENST00000264870.7:c.1315G=	ENSP00000264870.3:p.Asp439=
NM_000129.3:c.1315G= , LRG_549t1:c.1315G=	NP_000120.2:p.Asp439=
XM_006715010.2:c.1315G=	XP_006715073.1:p.Asp439=
XM_011514342.1:c.1477G=	XP_011512644.1:p.Asp493=
NM_000129.4:c.1315G= MANE Select	NP_000120.2:p.Asp439=