Canonical Allele Identifier: CA369855179

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646071A>T (hg19) ; chr7:g.150948983A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948983A>T , CM000669.2:g.150948983A>T	GRCh38
NC_000007.13:g.150646071A>T , CM000669.1:g.150646071A>T	GRCh37
NC_000007.12:g.150277004A>T	NCBI36
NG_008916.1:g.33944T>A , LRG_288:g.33944T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3298T>A
ENST00000262186.10:c.2465T>A MANE Select	ENSP00000262186.5:p.Val822Glu
ENST00000330883.9:c.1445T>A	ENSP00000328531.4:p.Val482Glu
ENST00000262186.9:c.2465T>A	ENSP00000262186.5:p.Val822Glu
ENST00000330883.8:c.1445T>A	ENSP00000328531.4:p.Val482Glu
NM_000238.3:c.2465T>A , LRG_288t1:c.2465T>A	NP_000229.1:p.Val822Glu
NM_172057.2:c.1445T>A , LRG_288t3:c.1445T>A	NP_742054.1:p.Val482Glu
XM_011516185.1:c.2165T>A	XP_011514487.1:p.Val722Glu
XM_011516186.1:c.2465T>A	XP_011514488.1:p.Val822Glu
XM_011516185.2:c.2165T>A	XP_011514487.1:p.Val722Glu
XM_011516186.3:c.2465T>A	XP_011514488.1:p.Val822Glu
XM_017012195.1:c.2315T>A	XP_016867684.1:p.Val772Glu
XM_017012196.1:c.2288T>A	XP_016867685.1:p.Val763Glu
NM_000238.4:c.2465T>A MANE Select	NP_000229.1:p.Val822Glu
NM_172057.3:c.1445T>A	NP_742054.1:p.Val482Glu