Canonical Allele Identifier: CA007042
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67418
dbSNP Id: rs199473495

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150974758A>G , CM000669.2:g.150974758A>G GRCh38
NC_000007.13:g.150671846A>G , CM000669.1:g.150671846A>G GRCh37
NC_000007.12:g.150302779A>G NCBI36
NG_008916.1:g.8169T>C , LRG_288:g.8169T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262186.10:c.260T>C MANE Select ENSP00000262186.5:p.Leu87Pro
ENST00000262186.9:c.260T>C ENSP00000262186.5:p.Leu87Pro
ENST00000430723.4:c.83T>C ENSP00000387657.4:p.Leu28Pro
ENST00000532957.5:n.483T>C
NM_000238.3:c.260T>C , LRG_288t1:c.260T>C NP_000229.1:p.Leu87Pro
NM_172056.2:c.260T>C , LRG_288t2:c.260T>C NP_742053.1:p.Leu87Pro
XM_011516186.1:c.260T>C XP_011514488.1:p.Leu87Pro
XM_011516186.3:c.260T>C XP_011514488.1:p.Leu87Pro
XM_017012196.1:c.83T>C XP_016867685.1:p.Leu28Pro
NM_000238.4:c.260T>C MANE Select NP_000229.1:p.Leu87Pro