Canonical Allele Identifier: CA2807641410

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713365del , CM000678.2:g.74713365del	GRCh38
NC_000016.9:g.74747263del , CM000678.1:g.74747263del	GRCh37
NC_000016.8:g.73304764del	NCBI36
NG_017070.1:g.66468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*826del MANE Select	ENSP00000219368.3:n.*826del
ENST00000219368.7:c.*826del	ENSP00000219368.3:n.*826del
ENST00000562145.1:n.1666del
NM_024306.4:c.*826del	NP_077282.3:n.*826del
XM_011523319.1:c.*826del	XP_011521621.1:n.*826del
XM_011523319.2:c.*826del	XP_011521621.1:n.*826del
NM_024306.5:c.*826del MANE Select	NP_077282.3:n.*826del