Canonical Allele Identifier: CA1607987882

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224815T= , CM000668.2:g.6224815T=	GRCh38
NC_000006.11:g.6225048T= , CM000668.1:g.6225048T=	GRCh37
NC_000006.10:g.6170047T=	NCBI36
NG_008107.1:g.100877A= , LRG_549:g.100877A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.844A= MANE Select	ENSP00000264870.3:p.Asn282=
ENST00000264870.7:c.844A=	ENSP00000264870.3:p.Asn282=
NM_000129.3:c.844A= , LRG_549t1:c.844A=	NP_000120.2:p.Asn282=
XM_006715010.2:c.844A=	XP_006715073.1:p.Asn282=
XM_011514342.1:c.1006A=	XP_011512644.1:p.Asn336=
NM_000129.4:c.844A= MANE Select	NP_000120.2:p.Asn282=