Canonical Allele Identifier: CA071338

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150950244-G-A
• MyVariant Identifiers: chr7:g.150647332G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950244G>A , CM000669.2:g.150950244G>A	GRCh38
NC_000007.13:g.150647332G>A , CM000669.1:g.150647332G>A	GRCh37
NC_000007.12:g.150278265G>A	NCBI36
NG_008916.1:g.32683C>T , LRG_288:g.32683C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1620C>T
ENST00000684241.1:n.3155C>T
ENST00000262186.10:c.2322C>T MANE Select	ENSP00000262186.5:p.Asp774=
ENST00000330883.9:c.1302C>T	ENSP00000328531.4:p.Asp434=
ENST00000262186.9:c.2322C>T	ENSP00000262186.5:p.Asp774=
ENST00000330883.8:c.1302C>T	ENSP00000328531.4:p.Asp434=
ENST00000430723.4:c.1974C>T	ENSP00000387657.4:p.Asp658=
ENST00000461280.1:n.1609C>T
ENST00000473610.5:n.1954C>T
ENST00000532957.5:n.2545C>T
NM_000238.3:c.2322C>T , LRG_288t1:c.2322C>T	NP_000229.1:p.Asp774=
NM_001204798.1:c.1302C>T	NP_001191727.1:p.Asp434=
NM_172056.2:c.2322C>T , LRG_288t2:c.2322C>T	NP_742053.1:p.Asp774=
NM_172057.2:c.1302C>T , LRG_288t3:c.1302C>T	NP_742054.1:p.Asp434=
XM_011516185.1:c.2022C>T	XP_011514487.1:p.Asp674=
XM_011516186.1:c.2322C>T	XP_011514488.1:p.Asp774=
XM_011516185.2:c.2022C>T	XP_011514487.1:p.Asp674=
XM_011516186.3:c.2322C>T	XP_011514488.1:p.Asp774=
XM_017012195.1:c.2172C>T	XP_016867684.1:p.Asp724=
XM_017012196.1:c.2145C>T	XP_016867685.1:p.Asp715=
NM_000238.4:c.2322C>T MANE Select	NP_000229.1:p.Asp774=
NM_001204798.2:c.1302C>T	NP_001191727.1:p.Asp434=
NM_172057.3:c.1302C>T	NP_742054.1:p.Asp434=