Canonical Allele Identifier: CA2807641411

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713367dup , CM000678.2:g.74713367dup	GRCh38
NC_000016.9:g.74747265dup , CM000678.1:g.74747265dup	GRCh37
NC_000016.8:g.73304766dup	NCBI36
NG_017070.1:g.66465dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*823dup MANE Select	ENSP00000219368.3:n.*823dup
ENST00000219368.7:c.*823dup	ENSP00000219368.3:n.*823dup
ENST00000562145.1:n.1663dup
NM_024306.4:c.*823dup	NP_077282.3:n.*823dup
XM_011523319.1:c.*823dup	XP_011521621.1:n.*823dup
XM_011523319.2:c.*823dup	XP_011521621.1:n.*823dup
NM_024306.5:c.*823dup MANE Select	NP_077282.3:n.*823dup