Canonical Allele Identifier: CA1162023555

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761422G= , CM000663.2:g.34761422G= GRCh38
NC_000001.10:g.35227023G= , CM000663.1:g.35227023G= GRCh37
NC_000001.9:g.34999610G= NCBI36
NG_016243.1:g.6682G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.168G= (GJB4) MANE Select ENSP00000345868.1:p.Lys56=
ENST00000339480.1:c.168G= (GJB4) ENSP00000345868.1:p.Lys56=
ENST00000426886.1:c.208-43013C= (SMIM12) ENSP00000429902.1:n.208-43013C=
NM_153212.2:c.168G= (GJB4) NP_694944.1:p.Lys56=
XM_011540679.1:c.168G= (GJB4) XP_011538981.1:p.Lys56=
XR_947179.1:n.1002-17973C=
XM_011540679.2:c.168G= (GJB4) XP_011538981.1:p.Lys56=
XR_001737967.1:n.1023+36949C=
NM_153212.3:c.168G= (GJB4) MANE Select NP_694944.1:p.Lys56=