Canonical Allele Identifier: CA1607949592

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145093T= , CM000668.2:g.6145093T=	GRCh38
NC_000006.11:g.6145326T= , CM000668.1:g.6145326T=	GRCh37
NC_000006.10:g.6090325T=	NCBI36
NG_008107.1:g.180599A= , LRG_549:g.180599A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*526A= MANE Select	ENSP00000264870.3:n.*526A=
ENST00000264870.7:c.*526A=	ENSP00000264870.3:n.*526A=
NM_000129.3:c.*526A= , LRG_549t1:c.*526A=	NP_000120.2:n.*526A=
XM_006715010.2:c.*526A=	XP_006715073.1:n.*526A=
XM_011514342.1:c.*526A=	XP_011512644.1:n.*526A=
NM_000129.4:c.*526A= MANE Select	NP_000120.2:n.*526A=