Canonical Allele Identifier: CA369860273

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150952805-G-A
• MyVariant Identifiers: chr7:g.150649893G>A (hg19) ; chr7:g.150952805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952805G>A , CM000669.2:g.150952805G>A	GRCh38
NC_000007.13:g.150649893G>A , CM000669.1:g.150649893G>A	GRCh37
NC_000007.12:g.150280826G>A	NCBI36
NG_008916.1:g.30122C>T , LRG_288:g.30122C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.475C>T
ENST00000684116.1:n.70C>T
ENST00000684241.1:n.2010C>T
ENST00000262186.10:c.1177C>T MANE Select	ENSP00000262186.5:p.Pro393Ser
ENST00000330883.9:c.157C>T	ENSP00000328531.4:p.Pro53Ser
ENST00000262186.9:c.1177C>T	ENSP00000262186.5:p.Pro393Ser
ENST00000330883.8:c.157C>T	ENSP00000328531.4:p.Pro53Ser
ENST00000430723.4:c.829C>T	ENSP00000387657.4:p.Pro277Ser
ENST00000461280.1:n.464C>T
ENST00000473610.5:n.482C>T
ENST00000532957.5:n.1400C>T
NM_000238.3:c.1177C>T , LRG_288t1:c.1177C>T	NP_000229.1:p.Pro393Ser
NM_001204798.1:c.157C>T	NP_001191727.1:p.Pro53Ser
NM_172056.2:c.1177C>T , LRG_288t2:c.1177C>T	NP_742053.1:p.Pro393Ser
NM_172057.2:c.157C>T , LRG_288t3:c.157C>T	NP_742054.1:p.Pro53Ser
XM_011516185.1:c.877C>T	XP_011514487.1:p.Pro293Ser
XM_011516186.1:c.1177C>T	XP_011514488.1:p.Pro393Ser
XM_011516185.2:c.877C>T	XP_011514487.1:p.Pro293Ser
XM_011516186.3:c.1177C>T	XP_011514488.1:p.Pro393Ser
XM_017012195.1:c.1027C>T	XP_016867684.1:p.Pro343Ser
XM_017012196.1:c.1000C>T	XP_016867685.1:p.Pro334Ser
NM_000238.4:c.1177C>T MANE Select	NP_000229.1:p.Pro393Ser
NM_001204798.2:c.157C>T	NP_001191727.1:p.Pro53Ser
NM_172057.3:c.157C>T	NP_742054.1:p.Pro53Ser