Canonical Allele Identifier: CA369853491

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1188698
• ClinVar RCV Id: RCV001548575
• dbSNP Id: rs2116933927
• gnomAD v4: 7-150947834-C-T
• MyVariant Identifiers: chr7:g.150644922C>T (hg19) ; chr7:g.150947834C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947834C>T , CM000669.2:g.150947834C>T	GRCh38
NC_000007.13:g.150644922C>T , CM000669.1:g.150644922C>T	GRCh37
NC_000007.12:g.150275855C>T	NCBI36
NG_008916.1:g.35093G>A , LRG_288:g.35093G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3570G>A
ENST00000262186.10:c.2737G>A MANE Select	ENSP00000262186.5:p.Ala913Thr
ENST00000330883.9:c.1717G>A	ENSP00000328531.4:p.Ala573Thr
ENST00000262186.9:c.2737G>A	ENSP00000262186.5:p.Ala913Thr
ENST00000330883.8:c.1717G>A	ENSP00000328531.4:p.Ala573Thr
NM_000238.3:c.2737G>A , LRG_288t1:c.2737G>A	NP_000229.1:p.Ala913Thr
NM_172057.2:c.1717G>A , LRG_288t3:c.1717G>A	NP_742054.1:p.Ala573Thr
XM_011516185.1:c.2437G>A	XP_011514487.1:p.Ala813Thr
XM_011516186.1:c.2693-143G>A	XP_011514488.1:n.2693-143G>A
XM_011516185.2:c.2437G>A	XP_011514487.1:p.Ala813Thr
XM_011516186.3:c.2693-143G>A	XP_011514488.1:n.2693-143G>A
XM_017012195.1:c.2587G>A	XP_016867684.1:p.Ala863Thr
XM_017012196.1:c.2560G>A	XP_016867685.1:p.Ala854Thr
NM_000238.4:c.2737G>A MANE Select	NP_000229.1:p.Ala913Thr
NM_172057.3:c.1717G>A	NP_742054.1:p.Ala573Thr