Canonical Allele Identifier: CA2685610008

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150952404-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952404C>G , CM000669.2:g.150952404C>G	GRCh38
NC_000007.13:g.150649492C>G , CM000669.1:g.150649492C>G	GRCh37
NC_000007.12:g.150280425C>G	NCBI36
NG_008916.1:g.30523G>C , LRG_288:g.30523G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.855+21G>C
ENST00000684116.1:n.450+21G>C
ENST00000684241.1:n.2390+21G>C
ENST00000262186.10:c.1557+21G>C MANE Select	ENSP00000262186.5:n.1557+21G>C
ENST00000330883.9:c.537+21G>C	ENSP00000328531.4:n.537+21G>C
ENST00000262186.9:c.1557+21G>C	ENSP00000262186.5:n.1557+21G>C
ENST00000330883.8:c.537+21G>C	ENSP00000328531.4:n.537+21G>C
ENST00000430723.4:c.1209+21G>C	ENSP00000387657.4:n.1209+21G>C
ENST00000461280.1:n.844+21G>C
ENST00000473610.5:n.862+21G>C
ENST00000532957.5:n.1780+21G>C
NM_000238.3:c.1557+21G>C , LRG_288t1:c.1557+21G>C	NP_000229.1:n.1557+21G>C
NM_001204798.1:c.537+21G>C	NP_001191727.1:n.537+21G>C
NM_172056.2:c.1557+21G>C , LRG_288t2:c.1557+21G>C	NP_742053.1:n.1557+21G>C
NM_172057.2:c.537+21G>C , LRG_288t3:c.537+21G>C	NP_742054.1:n.537+21G>C
XM_011516185.1:c.1257+21G>C	XP_011514487.1:n.1257+21G>C
XM_011516186.1:c.1557+21G>C	XP_011514488.1:n.1557+21G>C
XM_011516185.2:c.1257+21G>C	XP_011514487.1:n.1257+21G>C
XM_011516186.3:c.1557+21G>C	XP_011514488.1:n.1557+21G>C
XM_017012195.1:c.1407+21G>C	XP_016867684.1:n.1407+21G>C
XM_017012196.1:c.1380+21G>C	XP_016867685.1:n.1380+21G>C
NM_000238.4:c.1557+21G>C MANE Select	NP_000229.1:n.1557+21G>C
NM_001204798.2:c.537+21G>C	NP_001191727.1:n.537+21G>C
NM_172057.3:c.537+21G>C	NP_742054.1:n.537+21G>C