Canonical Allele Identifier: CA2685601400

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947230-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947230G>T , CM000669.2:g.150947230G>T	GRCh38
NC_000007.13:g.150644318G>T , CM000669.1:g.150644318G>T	GRCh37
NC_000007.12:g.150275251G>T	NCBI36
NG_008916.1:g.35697C>A , LRG_288:g.35697C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3985+98C>A
ENST00000262186.10:c.3152+98C>A MANE Select	ENSP00000262186.5:n.3152+98C>A
ENST00000330883.9:c.2132+98C>A	ENSP00000328531.4:n.2132+98C>A
ENST00000262186.9:c.3152+98C>A	ENSP00000262186.5:n.3152+98C>A
ENST00000330883.8:c.2132+98C>A	ENSP00000328531.4:n.2132+98C>A
NM_000238.3:c.3152+98C>A , LRG_288t1:c.3152+98C>A	NP_000229.1:n.3152+98C>A
NM_172057.2:c.2132+98C>A , LRG_288t3:c.2132+98C>A	NP_742054.1:n.2132+98C>A
XM_011516185.1:c.2852+98C>A	XP_011514487.1:n.2852+98C>A
XM_011516185.2:c.2852+98C>A	XP_011514487.1:n.2852+98C>A
XM_017012195.1:c.3002+98C>A	XP_016867684.1:n.3002+98C>A
XM_017012196.1:c.2975+98C>A	XP_016867685.1:n.2975+98C>A
NM_000238.4:c.3152+98C>A MANE Select	NP_000229.1:n.3152+98C>A
NM_172057.3:c.2132+98C>A	NP_742054.1:n.2132+98C>A