Canonical Allele Identifier: CA1139889799
Community Standard Title: NM_002060.3(GJA4):c.955C= (p.Pro319=)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34795168C= , CM000663.2:g.34795168C= GRCh38
NC_000001.10:g.35260769C= , CM000663.1:g.35260769C= GRCh37
NC_000001.9:g.35033356C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002060.3:c.955C= (GJA4) MANE Select NP_002051.2:p.Pro319=
ENST00000342280.5:c.955C= (GJA4) MANE Select ENSP00000343676.4:p.Pro319=
NM_002060.2:c.955C= (GJA4) NP_002051.2:p.Pro319=
ENST00000342280.4:c.955C= (GJA4) ENSP00000343676.4:p.Pro319=
ENST00000426886.1:c.207+60603G= (SMIM12) ENSP00000429902.1:n.207+60603G=
XM_005270750.1:c.955C= (GJA4) XP_005270807.1:p.Pro319=
XM_005270750.2:c.955C= (GJA4) XP_005270807.1:p.Pro319=
XM_017001043.2:c.955C= (GJA4) XP_016856532.1:p.Pro319=
XR_001737967.1:n.1023+3203G=
XR_947179.1:n.1001+3203G=