Canonical Allele Identifier: CA2232965646

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74726326C= , CM000678.2:g.74726326C=	GRCh38
NC_000016.9:g.74760224C= , CM000678.1:g.74760224C=	GRCh37
NC_000016.8:g.73317725C=	NCBI36
NG_017070.1:g.53506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.512G= MANE Select	ENSP00000219368.3:p.Ser171=
ENST00000219368.7:c.512G=	ENSP00000219368.3:p.Ser171=
ENST00000567683.5:c.364-7166G=	ENSP00000455126.1:n.364-7166G=
ENST00000569949.1:c.314G=	ENSP00000464576.1:p.Ser105=
NM_024306.4:c.512G=	NP_077282.3:p.Ser171=
XM_011523317.1:c.512G=	XP_011521619.1:p.Ser171=
XM_011523318.1:c.512G=	XP_011521620.1:p.Ser171=
XM_011523319.1:c.272G=	XP_011521621.1:p.Ser91=
XM_011523317.3:c.512G=	XP_011521619.1:p.Ser171=
XM_011523319.2:c.272G=	XP_011521621.1:p.Ser91=
NM_024306.5:c.512G= MANE Select	NP_077282.3:p.Ser171=