Canonical Allele Identifier: CA2077139478
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189246_20189248delinsCTT , CM000675.2:g.20189246_20189248delinsCTT GRCh38
NC_000013.10:g.20763385_20763387delinsCTT , CM000675.1:g.20763385_20763387delinsCTT GRCh37
NC_000013.9:g.19661385_19661387delinsCTT NCBI36
NG_008358.1:g.8728_8730delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.334_336delinsAAG ENSP00000372295.1:p.Lys112=
ENST00000382848.5:c.334_336delinsAAG MANE Select ENSP00000372299.4:p.Lys112=
ENST00000382844.1:c.334_336delinsAAG ENSP00000372295.1:p.Lys112=
ENST00000382848.4:c.334_336delinsAAG ENSP00000372299.4:p.Lys112=
NM_004004.5:c.334_336delinsAAG NP_003995.2:p.Lys112=
XM_011535049.1:c.334_336delinsAAG XP_011533351.1:p.Lys112=
XM_011535049.2:c.334_336delinsAAG XP_011533351.1:p.Lys112=
NM_004004.6:c.334_336delinsAAG MANE Select NP_003995.2:p.Lys112=