Canonical Allele Identifier: CA2579062540

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948353-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948353C>T , CM000669.2:g.150948353C>T	GRCh38
NC_000007.13:g.150645441C>T , CM000669.1:g.150645441C>T	GRCh37
NC_000007.12:g.150276374C>T	NCBI36
NG_008916.1:g.34574G>A , LRG_288:g.34574G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3525+91G>A
ENST00000262186.10:c.2692+91G>A MANE Select	ENSP00000262186.5:n.2692+91G>A
ENST00000330883.9:c.1672+91G>A	ENSP00000328531.4:n.1672+91G>A
ENST00000262186.9:c.2692+91G>A	ENSP00000262186.5:n.2692+91G>A
ENST00000330883.8:c.1672+91G>A	ENSP00000328531.4:n.1672+91G>A
NM_000238.3:c.2692+91G>A , LRG_288t1:c.2692+91G>A	NP_000229.1:n.2692+91G>A
NM_172057.2:c.1672+91G>A , LRG_288t3:c.1672+91G>A	NP_742054.1:n.1672+91G>A
XM_011516185.1:c.2392+91G>A	XP_011514487.1:n.2392+91G>A
XM_011516186.1:c.2692+91G>A	XP_011514488.1:n.2692+91G>A
XM_011516185.2:c.2392+91G>A	XP_011514487.1:n.2392+91G>A
XM_011516186.3:c.2692+91G>A	XP_011514488.1:n.2692+91G>A
XM_017012195.1:c.2542+91G>A	XP_016867684.1:n.2542+91G>A
XM_017012196.1:c.2515+91G>A	XP_016867685.1:n.2515+91G>A
NM_000238.4:c.2692+91G>A MANE Select	NP_000229.1:n.2692+91G>A
NM_172057.3:c.1672+91G>A	NP_742054.1:n.1672+91G>A