Canonical Allele Identifier: CA2634286128

Gene: FA2H

Linked Data

• gnomAD v4: 16-74713299-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713302del , CM000678.2:g.74713302del	GRCh38
NC_000016.9:g.74747200del , CM000678.1:g.74747200del	GRCh37
NC_000016.8:g.73304701del	NCBI36
NG_017070.1:g.66532del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*890del MANE Select	ENSP00000219368.3:n.*890del
ENST00000219368.7:c.*890del	ENSP00000219368.3:n.*890del
ENST00000562145.1:n.1730del
NM_024306.4:c.*890del	NP_077282.3:n.*890del
XM_011523319.1:c.*890del	XP_011521621.1:n.*890del
XM_011523319.2:c.*890del	XP_011521621.1:n.*890del
NM_024306.5:c.*890del MANE Select	NP_077282.3:n.*890del