Canonical Allele Identifier: CA2695217659
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189069_20189070insCGTT , CM000675.2:g.20189069_20189070insCGTT GRCh38
NC_000013.10:g.20763208_20763209insCGTT , CM000675.1:g.20763208_20763209insCGTT GRCh37
NC_000013.9:g.19661208_19661209insCGTT NCBI36
NG_008358.1:g.8906_8907insAACG

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.512_513insAACG ENSP00000372295.1:p.Trp172ThrfsTer?
ENST00000382848.5:c.512_513insAACG MANE Select ENSP00000372299.4:p.Trp172ThrfsTer?
ENST00000382844.1:c.512_513insAACG ENSP00000372295.1:p.Trp172ThrfsTer?
ENST00000382848.4:c.512_513insAACG ENSP00000372299.4:p.Trp172ThrfsTer?
NM_004004.5:c.512_513insAACG NP_003995.2:p.Trp172ThrfsTer?
XM_011535049.1:c.512_513insAACG XP_011533351.1:p.Trp172ThrfsTer?
XM_011535049.2:c.512_513insAACG XP_011533351.1:p.Trp172ThrfsTer?
NM_004004.6:c.512_513insAACG MANE Select NP_003995.2:p.Trp172ThrfsTer?