Canonical Allele Identifier: CA2232953694

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74719071G= , CM000678.2:g.74719071G=	GRCh38
NC_000016.9:g.74752969G= , CM000678.1:g.74752969G=	GRCh37
NC_000016.8:g.73310470G=	NCBI36
NG_017070.1:g.60761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.703C= MANE Select	ENSP00000219368.3:p.Arg235=
ENST00000219368.7:c.703C=	ENSP00000219368.3:p.Arg235=
ENST00000567683.5:c.453C=	ENSP00000455126.1:p.Thr151=
ENST00000569949.1:c.505C=	ENSP00000464576.1:p.Arg169=
NM_024306.4:c.703C=	NP_077282.3:p.Arg235=
XM_011523317.1:c.703C=	XP_011521619.1:p.Arg235=
XM_011523318.1:c.703C=	XP_011521620.1:p.Arg235=
XM_011523319.1:c.463C=	XP_011521621.1:p.Arg155=
XM_011523317.3:c.703C=	XP_011521619.1:p.Arg235=
XM_011523319.2:c.463C=	XP_011521621.1:p.Arg155=
NM_024306.5:c.703C= MANE Select	NP_077282.3:p.Arg235=