Canonical Allele Identifier: CA458646979

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656802C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959714C>A , CM000669.2:g.150959714C>A	GRCh38
NC_000007.13:g.150656802C>A , CM000669.1:g.150656802C>A	GRCh37
NC_000007.12:g.150287735C>A	NCBI36
NG_008916.1:g.23213G>T , LRG_288:g.23213G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1163G>T
ENST00000262186.10:c.330G>T MANE Select	ENSP00000262186.5:p.Val110=
ENST00000262186.9:c.330G>T	ENSP00000262186.5:p.Val110=
ENST00000430723.4:c.153G>T	ENSP00000387657.4:p.Val51=
ENST00000532957.5:n.553G>T
NM_000238.3:c.330G>T , LRG_288t1:c.330G>T	NP_000229.1:p.Val110=
NM_172056.2:c.330G>T , LRG_288t2:c.330G>T	NP_742053.1:p.Val110=
XM_011516185.1:c.30G>T	XP_011514487.1:p.Val10=
XM_011516186.1:c.330G>T	XP_011514488.1:p.Val110=
XM_011516185.2:c.30G>T	XP_011514487.1:p.Val10=
XM_011516186.3:c.330G>T	XP_011514488.1:p.Val110=
XM_017012195.1:c.180G>T	XP_016867684.1:p.Val60=
XM_017012196.1:c.153G>T	XP_016867685.1:p.Val51=
NM_000238.4:c.330G>T MANE Select	NP_000229.1:p.Val110=