Canonical Allele Identifier: CA1162023558

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761426C= , CM000663.2:g.34761426C= GRCh38
NC_000001.10:g.35227027C= , CM000663.1:g.35227027C= GRCh37
NC_000001.9:g.34999614C= NCBI36
NG_016243.1:g.6686C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.172C= (GJB4) MANE Select ENSP00000345868.1:p.Pro58=
ENST00000339480.1:c.172C= (GJB4) ENSP00000345868.1:p.Pro58=
ENST00000426886.1:c.208-43017G= (SMIM12) ENSP00000429902.1:n.208-43017G=
NM_153212.2:c.172C= (GJB4) NP_694944.1:p.Pro58=
XM_011540679.1:c.172C= (GJB4) XP_011538981.1:p.Pro58=
XR_947179.1:n.1002-17977G=
XM_011540679.2:c.172C= (GJB4) XP_011538981.1:p.Pro58=
XR_001737967.1:n.1023+36945G=
NM_153212.3:c.172C= (GJB4) MANE Select NP_694944.1:p.Pro58=