Canonical Allele Identifier: CA2232921997

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713601_74713604delinsAACG , CM000678.2:g.74713601_74713604delinsAACG	GRCh38
NC_000016.9:g.74747499_74747502delinsAACG , CM000678.1:g.74747499_74747502delinsAACG	GRCh37
NC_000016.8:g.73305000_73305003delinsAACG	NCBI36
NG_017070.1:g.66228_66231delinsCGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*586_*589delinsCGTT MANE Select	ENSP00000219368.3:n.*586_*589delinsCGTT
ENST00000219368.7:c.*586_*589delinsCGTT	ENSP00000219368.3:n.*586_*589delinsCGTT
ENST00000562145.1:n.1426_1429delinsCGTT
ENST00000567683.5:c.*984_*987delinsCGTT	ENSP00000455126.1:n.*984_*987delinsCGTT
NM_024306.4:c.*586_*589delinsCGTT	NP_077282.3:n.*586_*589delinsCGTT
XM_011523319.1:c.*586_*589delinsCGTT	XP_011521621.1:n.*586_*589delinsCGTT
XM_011523319.2:c.*586_*589delinsCGTT	XP_011521621.1:n.*586_*589delinsCGTT
NM_024306.5:c.*586_*589delinsCGTT MANE Select	NP_077282.3:n.*586_*589delinsCGTT