Canonical Allele Identifier: CA1607949811

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145623A= , CM000668.2:g.6145623A=	GRCh38
NC_000006.11:g.6145856A= , CM000668.1:g.6145856A=	GRCh37
NC_000006.10:g.6090855A=	NCBI36
NG_008107.1:g.180069T= , LRG_549:g.180069T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.2195T= MANE Select	ENSP00000264870.3:p.Met732=
ENST00000264870.7:c.2195T=	ENSP00000264870.3:p.Met732=
NM_000129.3:c.2195T= , LRG_549t1:c.2195T=	NP_000120.2:p.Met732=
XM_006715010.2:c.2195T=	XP_006715073.1:p.Met732=
XM_011514342.1:c.2357T=	XP_011512644.1:p.Met786=
NM_000129.4:c.2195T= MANE Select	NP_000120.2:p.Met732=