Canonical Allele Identifier: CA458871668

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649705C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952617C>G , CM000669.2:g.150952617C>G	GRCh38
NC_000007.13:g.150649705C>G , CM000669.1:g.150649705C>G	GRCh37
NC_000007.12:g.150280638C>G	NCBI36
NG_008916.1:g.30310G>C , LRG_288:g.30310G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.663G>C
ENST00000684116.1:n.258G>C
ENST00000684241.1:n.2198G>C
ENST00000262186.10:c.1365G>C MANE Select	ENSP00000262186.5:p.Val455=
ENST00000330883.9:c.345G>C	ENSP00000328531.4:p.Val115=
ENST00000262186.9:c.1365G>C	ENSP00000262186.5:p.Val455=
ENST00000330883.8:c.345G>C	ENSP00000328531.4:p.Val115=
ENST00000430723.4:c.1017G>C	ENSP00000387657.4:p.Val339=
ENST00000461280.1:n.652G>C
ENST00000473610.5:n.670G>C
ENST00000532957.5:n.1588G>C
NM_000238.3:c.1365G>C , LRG_288t1:c.1365G>C	NP_000229.1:p.Val455=
NM_001204798.1:c.345G>C	NP_001191727.1:p.Val115=
NM_172056.2:c.1365G>C , LRG_288t2:c.1365G>C	NP_742053.1:p.Val455=
NM_172057.2:c.345G>C , LRG_288t3:c.345G>C	NP_742054.1:p.Val115=
XM_011516185.1:c.1065G>C	XP_011514487.1:p.Val355=
XM_011516186.1:c.1365G>C	XP_011514488.1:p.Val455=
XM_011516185.2:c.1065G>C	XP_011514487.1:p.Val355=
XM_011516186.3:c.1365G>C	XP_011514488.1:p.Val455=
XM_017012195.1:c.1215G>C	XP_016867684.1:p.Val405=
XM_017012196.1:c.1188G>C	XP_016867685.1:p.Val396=
NM_000238.4:c.1365G>C MANE Select	NP_000229.1:p.Val455=
NM_001204798.2:c.345G>C	NP_001191727.1:p.Val115=
NM_172057.3:c.345G>C	NP_742054.1:p.Val115=