Canonical Allele Identifier: CA369855408

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646139T>A (hg19) ; chr7:g.150949051T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949051T>A , CM000669.2:g.150949051T>A	GRCh38
NC_000007.13:g.150646139T>A , CM000669.1:g.150646139T>A	GRCh37
NC_000007.12:g.150277072T>A	NCBI36
NG_008916.1:g.33876A>T , LRG_288:g.33876A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3232-2A>T
ENST00000262186.10:c.2399-2A>T MANE Select	ENSP00000262186.5:n.2399-2A>T
ENST00000330883.9:c.1379-2A>T	ENSP00000328531.4:n.1379-2A>T
ENST00000262186.9:c.2399-2A>T	ENSP00000262186.5:n.2399-2A>T
ENST00000330883.8:c.1379-2A>T	ENSP00000328531.4:n.1379-2A>T
NM_000238.3:c.2399-2A>T , LRG_288t1:c.2399-2A>T	NP_000229.1:n.2399-2A>T
NM_172057.2:c.1379-2A>T , LRG_288t3:c.1379-2A>T	NP_742054.1:n.1379-2A>T
XM_011516185.1:c.2099-2A>T	XP_011514487.1:n.2099-2A>T
XM_011516186.1:c.2399-2A>T	XP_011514488.1:n.2399-2A>T
XM_011516185.2:c.2099-2A>T	XP_011514487.1:n.2099-2A>T
XM_011516186.3:c.2399-2A>T	XP_011514488.1:n.2399-2A>T
XM_017012195.1:c.2249-2A>T	XP_016867684.1:n.2249-2A>T
XM_017012196.1:c.2222-2A>T	XP_016867685.1:n.2222-2A>T
NM_000238.4:c.2399-2A>T MANE Select	NP_000229.1:n.2399-2A>T
NM_172057.3:c.1379-2A>T	NP_742054.1:n.1379-2A>T