Canonical Allele Identifier: CA2232953721

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74719083A= , CM000678.2:g.74719083A=	GRCh38
NC_000016.9:g.74752981A= , CM000678.1:g.74752981A=	GRCh37
NC_000016.8:g.73310482A=	NCBI36
NG_017070.1:g.60749T=

Transcript Alleles

HGVS	Amino-acid Change
NM_024306.5:c.691T= MANE Select	NP_077282.3:p.Tyr231=
ENST00000219368.8:c.691T= MANE Select	ENSP00000219368.3:p.Tyr231=
NM_024306.4:c.691T=	NP_077282.3:p.Tyr231=
ENST00000219368.7:c.691T=	ENSP00000219368.3:p.Tyr231=
ENST00000567683.5:c.441T=	ENSP00000455126.1:p.Ser147=
ENST00000569949.1:c.493T=	ENSP00000464576.1:p.Tyr165=
XM_011523317.1:c.691T=	XP_011521619.1:p.Tyr231=
XM_011523317.3:c.691T=	XP_011521619.1:p.Tyr231=
XM_011523318.1:c.691T=	XP_011521620.1:p.Tyr231=
XM_011523319.1:c.451T=	XP_011521621.1:p.Tyr151=
XM_011523319.2:c.451T=	XP_011521621.1:p.Tyr151=