Canonical Allele Identifier: CA417127350

Linked Data

MyVariant Identifiers: chr1:g.35260774A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34795173A>G , CM000663.2:g.34795173A>G GRCh38
NC_000001.10:g.35260774A>G , CM000663.1:g.35260774A>G GRCh37
NC_000001.9:g.35033361A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000342280.5:c.960A>G (GJA4) MANE Select ENSP00000343676.4:p.Pro320=
ENST00000342280.4:c.960A>G (GJA4) ENSP00000343676.4:p.Pro320=
ENST00000426886.1:c.207+60598T>C (SMIM12) ENSP00000429902.1:n.207+60598T>C
NM_002060.2:c.960A>G (GJA4) NP_002051.2:p.Pro320=
XM_005270750.1:c.960A>G (GJA4) XP_005270807.1:p.Pro320=
XR_947179.1:n.1001+3198T>C
XM_005270750.2:c.960A>G (GJA4) XP_005270807.1:p.Pro320=
XM_017001043.2:c.960A>G (GJA4) XP_016856532.1:p.Pro320=
XR_001737967.1:n.1023+3198T>C
NM_002060.3:c.960A>G (GJA4) MANE Select NP_002051.2:p.Pro320=