Canonical Allele Identifier: CA369860282

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649897C>A (hg19) ; chr7:g.150952809C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952809C>A , CM000669.2:g.150952809C>A	GRCh38
NC_000007.13:g.150649897C>A , CM000669.1:g.150649897C>A	GRCh37
NC_000007.12:g.150280830C>A	NCBI36
NG_008916.1:g.30118G>T , LRG_288:g.30118G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.471G>T
ENST00000684116.1:n.66G>T
ENST00000684241.1:n.2006G>T
ENST00000262186.10:c.1173G>T MANE Select	ENSP00000262186.5:p.Gln391His
ENST00000330883.9:c.153G>T	ENSP00000328531.4:p.Gln51His
ENST00000262186.9:c.1173G>T	ENSP00000262186.5:p.Gln391His
ENST00000330883.8:c.153G>T	ENSP00000328531.4:p.Gln51His
ENST00000430723.4:c.825G>T	ENSP00000387657.4:p.Gln275His
ENST00000461280.1:n.460G>T
ENST00000473610.5:n.478G>T
ENST00000532957.5:n.1396G>T
NM_000238.3:c.1173G>T , LRG_288t1:c.1173G>T	NP_000229.1:p.Gln391His
NM_001204798.1:c.153G>T	NP_001191727.1:p.Gln51His
NM_172056.2:c.1173G>T , LRG_288t2:c.1173G>T	NP_742053.1:p.Gln391His
NM_172057.2:c.153G>T , LRG_288t3:c.153G>T	NP_742054.1:p.Gln51His
XM_011516185.1:c.873G>T	XP_011514487.1:p.Gln291His
XM_011516186.1:c.1173G>T	XP_011514488.1:p.Gln391His
XM_011516185.2:c.873G>T	XP_011514487.1:p.Gln291His
XM_011516186.3:c.1173G>T	XP_011514488.1:p.Gln391His
XM_017012195.1:c.1023G>T	XP_016867684.1:p.Gln341His
XM_017012196.1:c.996G>T	XP_016867685.1:p.Gln332His
NM_000238.4:c.1173G>T MANE Select	NP_000229.1:p.Gln391His
NM_001204798.2:c.153G>T	NP_001191727.1:p.Gln51His
NM_172057.3:c.153G>T	NP_742054.1:p.Gln51His