Canonical Allele Identifier: CA339322909

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794470G>T , CM000663.2:g.34794470G>T GRCh38
NC_000001.10:g.35260071G>T , CM000663.1:g.35260071G>T GRCh37
NC_000001.9:g.35032658G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.257G>T (GJA4) MANE Select ENSP00000343676.4:p.Ser86Ile
ENST00000342280.4:c.257G>T (GJA4) ENSP00000343676.4:p.Ser86Ile
ENST00000426886.1:c.207+61301C>A (SMIM12) ENSP00000429902.1:n.207+61301C>A
ENST00000450137.1:c.257G>T (GJA4) ENSP00000409186.1:p.Ser86Ile
NM_002060.2:c.257G>T (GJA4) NP_002051.2:p.Ser86Ile
XM_005270750.1:c.257G>T (GJA4) XP_005270807.1:p.Ser86Ile
XR_947179.1:n.1001+3901C>A
XM_005270750.2:c.257G>T (GJA4) XP_005270807.1:p.Ser86Ile
XM_017001043.2:c.257G>T (GJA4) XP_016856532.1:p.Ser86Ile
XR_001737967.1:n.1023+3901C>A
NM_002060.3:c.257G>T (GJA4) MANE Select NP_002051.2:p.Ser86Ile