Canonical Allele Identifier: CA2634286325

Gene: FA2H

Linked Data

• gnomAD v4: 16-74713367-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713372dup , CM000678.2:g.74713372dup	GRCh38
NC_000016.9:g.74747270dup , CM000678.1:g.74747270dup	GRCh37
NC_000016.8:g.73304771dup	NCBI36
NG_017070.1:g.66464dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*822dup MANE Select	ENSP00000219368.3:n.*822dup
ENST00000219368.7:c.*822dup	ENSP00000219368.3:n.*822dup
ENST00000562145.1:n.1662dup
NM_024306.4:c.*822dup	NP_077282.3:n.*822dup
XM_011523319.1:c.*822dup	XP_011521621.1:n.*822dup
XM_011523319.2:c.*822dup	XP_011521621.1:n.*822dup
NM_024306.5:c.*822dup MANE Select	NP_077282.3:n.*822dup