Canonical Allele Identifier: CA2644771049

Linked Data

gnomAD v4: 1-34794065-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794065C>T , CM000663.2:g.34794065C>T GRCh38
NC_000001.10:g.35259666C>T , CM000663.1:g.35259666C>T GRCh37
NC_000001.9:g.35032253C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.-17-132C>T (GJA4) MANE Select ENSP00000343676.4:n.-17-132C>T
ENST00000342280.4:c.-17-132C>T (GJA4) ENSP00000343676.4:n.-17-132C>T
ENST00000426886.1:c.207+61706G>A (SMIM12) ENSP00000429902.1:n.207+61706G>A
ENST00000450137.1:c.-112-37C>T (GJA4) ENSP00000409186.1:n.-112-37C>T
NM_002060.2:c.-17-132C>T (GJA4) NP_002051.2:n.-17-132C>T
XM_005270750.1:c.-112-37C>T (GJA4) XP_005270807.1:n.-112-37C>T
XR_947179.1:n.1001+4306G>A
XM_005270750.2:c.-112-37C>T (GJA4) XP_005270807.1:n.-112-37C>T
XM_017001043.2:c.-17-132C>T (GJA4) XP_016856532.1:n.-17-132C>T
XR_001737967.1:n.1023+4306G>A
NM_002060.3:c.-17-132C>T (GJA4) MANE Select NP_002051.2:n.-17-132C>T