Canonical Allele Identifier: CA369860023

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649764T>G (hg19) ; chr7:g.150952676T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952676T>G , CM000669.2:g.150952676T>G	GRCh38
NC_000007.13:g.150649764T>G , CM000669.1:g.150649764T>G	GRCh37
NC_000007.12:g.150280697T>G	NCBI36
NG_008916.1:g.30251A>C , LRG_288:g.30251A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.604A>C
ENST00000684116.1:n.199A>C
ENST00000684241.1:n.2139A>C
ENST00000262186.10:c.1306A>C MANE Select	ENSP00000262186.5:p.Thr436Pro
ENST00000330883.9:c.286A>C	ENSP00000328531.4:p.Thr96Pro
ENST00000262186.9:c.1306A>C	ENSP00000262186.5:p.Thr436Pro
ENST00000330883.8:c.286A>C	ENSP00000328531.4:p.Thr96Pro
ENST00000430723.4:c.958A>C	ENSP00000387657.4:p.Thr320Pro
ENST00000461280.1:n.593A>C
ENST00000473610.5:n.611A>C
ENST00000532957.5:n.1529A>C
NM_000238.3:c.1306A>C , LRG_288t1:c.1306A>C	NP_000229.1:p.Thr436Pro
NM_001204798.1:c.286A>C	NP_001191727.1:p.Thr96Pro
NM_172056.2:c.1306A>C , LRG_288t2:c.1306A>C	NP_742053.1:p.Thr436Pro
NM_172057.2:c.286A>C , LRG_288t3:c.286A>C	NP_742054.1:p.Thr96Pro
XM_011516185.1:c.1006A>C	XP_011514487.1:p.Thr336Pro
XM_011516186.1:c.1306A>C	XP_011514488.1:p.Thr436Pro
XM_011516185.2:c.1006A>C	XP_011514487.1:p.Thr336Pro
XM_011516186.3:c.1306A>C	XP_011514488.1:p.Thr436Pro
XM_017012195.1:c.1156A>C	XP_016867684.1:p.Thr386Pro
XM_017012196.1:c.1129A>C	XP_016867685.1:p.Thr377Pro
NM_000238.4:c.1306A>C MANE Select	NP_000229.1:p.Thr436Pro
NM_001204798.2:c.286A>C	NP_001191727.1:p.Thr96Pro
NM_172057.3:c.286A>C	NP_742054.1:p.Thr96Pro