Canonical Allele Identifier: CA1607987883

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224816G= , CM000668.2:g.6224816G=	GRCh38
NC_000006.11:g.6225049G= , CM000668.1:g.6225049G=	GRCh37
NC_000006.10:g.6170048G=	NCBI36
NG_008107.1:g.100876C= , LRG_549:g.100876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.843C= MANE Select	ENSP00000264870.3:p.Asp281=
ENST00000264870.7:c.843C=	ENSP00000264870.3:p.Asp281=
NM_000129.3:c.843C= , LRG_549t1:c.843C=	NP_000120.2:p.Asp281=
XM_006715010.2:c.843C=	XP_006715073.1:p.Asp281=
XM_011514342.1:c.1005C=	XP_011512644.1:p.Asp335=
NM_000129.4:c.843C= MANE Select	NP_000120.2:p.Asp281=