Canonical Allele Identifier: CA417248971

Linked Data

MyVariant Identifiers: chr1:g.35259862G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794261G>A , CM000663.2:g.34794261G>A GRCh38
NC_000001.10:g.35259862G>A , CM000663.1:g.35259862G>A GRCh37
NC_000001.9:g.35032449G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000342280.5:c.48G>A (GJA4) MANE Select ENSP00000343676.4:p.Glu16=
ENST00000342280.4:c.48G>A (GJA4) ENSP00000343676.4:p.Glu16=
ENST00000426886.1:c.207+61510C>T (SMIM12) ENSP00000429902.1:n.207+61510C>T
ENST00000450137.1:c.48G>A (GJA4) ENSP00000409186.1:p.Glu16=
NM_002060.2:c.48G>A (GJA4) NP_002051.2:p.Glu16=
XM_005270750.1:c.48G>A (GJA4) XP_005270807.1:p.Glu16=
XR_947179.1:n.1001+4110C>T
XM_005270750.2:c.48G>A (GJA4) XP_005270807.1:p.Glu16=
XM_017001043.2:c.48G>A (GJA4) XP_016856532.1:p.Glu16=
XR_001737967.1:n.1023+4110C>T
NM_002060.3:c.48G>A (GJA4) MANE Select NP_002051.2:p.Glu16=