Canonical Allele Identifier: CA1607973427

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182136G= , CM000668.2:g.6182136G=	GRCh38
NC_000006.11:g.6182369G= , CM000668.1:g.6182369G=	GRCh37
NC_000006.10:g.6127368G=	NCBI36
NG_008107.1:g.143556C= , LRG_549:g.143556C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1311C= MANE Select	ENSP00000264870.3:p.Asn437=
ENST00000264870.7:c.1311C=	ENSP00000264870.3:p.Asn437=
NM_000129.3:c.1311C= , LRG_549t1:c.1311C=	NP_000120.2:p.Asn437=
XM_006715010.2:c.1311C=	XP_006715073.1:p.Asn437=
XM_011514342.1:c.1473C=	XP_011512644.1:p.Asn491=
NM_000129.4:c.1311C= MANE Select	NP_000120.2:p.Asn437=