Canonical Allele Identifier: CA2232965662

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74726328G= , CM000678.2:g.74726328G=	GRCh38
NC_000016.9:g.74760226G= , CM000678.1:g.74760226G=	GRCh37
NC_000016.8:g.73317727G=	NCBI36
NG_017070.1:g.53504C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000219368.8:c.510C= MANE Select	ENSP00000219368.3:p.Tyr170=
ENST00000219368.7:c.510C=	ENSP00000219368.3:p.Tyr170=
ENST00000567683.5:c.364-7168C=	ENSP00000455126.1:n.364-7168C=
ENST00000569949.1:c.312C=	ENSP00000464576.1:p.Tyr104=
NM_024306.4:c.510C=	NP_077282.3:p.Tyr170=
XM_011523317.1:c.510C=	XP_011521619.1:p.Tyr170=
XM_011523318.1:c.510C=	XP_011521620.1:p.Tyr170=
XM_011523319.1:c.270C=	XP_011521621.1:p.Tyr90=
XM_011523317.3:c.510C=	XP_011521619.1:p.Tyr170=
XM_011523319.2:c.270C=	XP_011521621.1:p.Tyr90=
NM_024306.5:c.510C= MANE Select	NP_077282.3:p.Tyr170=