Canonical Allele Identifier: CA963888644
Gene: KCNH5 HGNC NCBI

Linked Data

dbSNP Id: rs8012941

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62855629A>T , CM000676.2:g.62855629A>T GRCh38
NC_000014.8:g.63322347A>T , CM000676.1:g.63322347A>T GRCh37
NC_000014.7:g.62392100A>T NCBI36
NG_034062.1:g.194610T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322893.12:c.1370-5777T>A MANE Select ENSP00000321427.7:n.1370-5777T>A
ENST00000322893.11:c.1370-5777T>A ENSP00000321427.7:n.1370-5777T>A
ENST00000394968.2:c.1196-5777T>A ENSP00000378419.1:n.1196-5777T>A
ENST00000420622.6:c.1370-5777T>A ENSP00000395439.2:n.1370-5777T>A
NM_139318.4:c.1370-5777T>A NP_647479.2:n.1370-5777T>A
NM_172375.2:c.1370-5777T>A NP_758963.1:n.1370-5777T>A
XM_011536658.1:c.1370-5777T>A XP_011534960.1:n.1370-5777T>A
NM_139318.5:c.1370-5777T>A MANE Select NP_647479.2:n.1370-5777T>A
NM_172375.3:c.1370-5777T>A NP_758963.1:n.1370-5777T>A