Canonical Allele Identifier: CA458871671

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649708C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952620C>G , CM000669.2:g.150952620C>G	GRCh38
NC_000007.13:g.150649708C>G , CM000669.1:g.150649708C>G	GRCh37
NC_000007.12:g.150280641C>G	NCBI36
NG_008916.1:g.30307G>C , LRG_288:g.30307G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.660G>C
ENST00000684116.1:n.255G>C
ENST00000684241.1:n.2195G>C
ENST00000262186.10:c.1362G>C MANE Select	ENSP00000262186.5:p.Val454=
ENST00000330883.9:c.342G>C	ENSP00000328531.4:p.Val114=
ENST00000262186.9:c.1362G>C	ENSP00000262186.5:p.Val454=
ENST00000330883.8:c.342G>C	ENSP00000328531.4:p.Val114=
ENST00000430723.4:c.1014G>C	ENSP00000387657.4:p.Val338=
ENST00000461280.1:n.649G>C
ENST00000473610.5:n.667G>C
ENST00000532957.5:n.1585G>C
NM_000238.3:c.1362G>C , LRG_288t1:c.1362G>C	NP_000229.1:p.Val454=
NM_001204798.1:c.342G>C	NP_001191727.1:p.Val114=
NM_172056.2:c.1362G>C , LRG_288t2:c.1362G>C	NP_742053.1:p.Val454=
NM_172057.2:c.342G>C , LRG_288t3:c.342G>C	NP_742054.1:p.Val114=
XM_011516185.1:c.1062G>C	XP_011514487.1:p.Val354=
XM_011516186.1:c.1362G>C	XP_011514488.1:p.Val454=
XM_011516185.2:c.1062G>C	XP_011514487.1:p.Val354=
XM_011516186.3:c.1362G>C	XP_011514488.1:p.Val454=
XM_017012195.1:c.1212G>C	XP_016867684.1:p.Val404=
XM_017012196.1:c.1185G>C	XP_016867685.1:p.Val395=
NM_000238.4:c.1362G>C MANE Select	NP_000229.1:p.Val454=
NM_001204798.2:c.342G>C	NP_001191727.1:p.Val114=
NM_172057.3:c.342G>C	NP_742054.1:p.Val114=