Canonical Allele Identifier: CA342397702
Gene: GJA5 HGNC NCBI

Linked Data

dbSNP Id: rs1663878598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147759025T>C , CM000663.2:g.147759025T>C GRCh38
NC_000001.10:g.147231133T>C , CM000663.1:g.147231133T>C GRCh37
NC_000001.9:g.145697757T>C NCBI36
NG_009369.2:g.19350A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000579774.3:c.214A>G MANE Select ENSP00000463851.1:p.Ile72Val
ENST00000430508.1:c.214A>G ENSP00000407645.1:p.Ile72Val
ENST00000579774.2:c.214A>G ENSP00000463851.1:p.Ile72Val
ENST00000621517.1:c.214A>G ENSP00000484552.1:p.Ile72Val
NM_005266.6:c.214A>G NP_005257.2:p.Ile72Val
NM_181703.3:c.214A>G NP_859054.1:p.Ile72Val
XM_005272951.3:c.214A>G XP_005273008.1:p.Ile72Val
XM_011509415.1:c.214A>G XP_011507717.1:p.Ile72Val
XR_922078.1:n.434-18536T>C
XR_922079.1:n.434-18536T>C
XM_005272951.4:c.214A>G XP_005273008.1:p.Ile72Val
XM_017001044.1:c.214A>G XP_016856533.1:p.Ile72Val
XR_922079.3:n.744-18536T>C
NM_181703.4:c.214A>G MANE Select NP_859054.1:p.Ile72Val
NM_005266.7:c.214A>G NP_005257.2:p.Ile72Val