Canonical Allele Identifier: CA1607949817

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145634T= , CM000668.2:g.6145634T=	GRCh38
NC_000006.11:g.6145867T= , CM000668.1:g.6145867T=	GRCh37
NC_000006.10:g.6090866T=	NCBI36
NG_008107.1:g.180058A= , LRG_549:g.180058A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.2184A= MANE Select	ENSP00000264870.3:p.Arg728=
ENST00000264870.7:c.2184A=	ENSP00000264870.3:p.Arg728=
NM_000129.3:c.2184A= , LRG_549t1:c.2184A=	NP_000120.2:p.Arg728=
XM_006715010.2:c.2184A=	XP_006715073.1:p.Arg728=
XM_011514342.1:c.2346A=	XP_011512644.1:p.Arg782=
NM_000129.4:c.2184A= MANE Select	NP_000120.2:p.Arg728=