Canonical Allele Identifier: CA369856729

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647498C>G (hg19) ; chr7:g.150950410C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950410C>G , CM000669.2:g.150950410C>G	GRCh38
NC_000007.13:g.150647498C>G , CM000669.1:g.150647498C>G	GRCh37
NC_000007.12:g.150278431C>G	NCBI36
NG_008916.1:g.32517G>C , LRG_288:g.32517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1454G>C
ENST00000684241.1:n.2989G>C
ENST00000262186.10:c.2156G>C MANE Select	ENSP00000262186.5:p.Gly719Ala
ENST00000330883.9:c.1136G>C	ENSP00000328531.4:p.Gly379Ala
ENST00000262186.9:c.2156G>C	ENSP00000262186.5:p.Gly719Ala
ENST00000330883.8:c.1136G>C	ENSP00000328531.4:p.Gly379Ala
ENST00000430723.4:c.1808G>C	ENSP00000387657.4:p.Gly603Ala
ENST00000461280.1:n.1443G>C
ENST00000473610.5:n.1788G>C
ENST00000532957.5:n.2379G>C
NM_000238.3:c.2156G>C , LRG_288t1:c.2156G>C	NP_000229.1:p.Gly719Ala
NM_001204798.1:c.1136G>C	NP_001191727.1:p.Gly379Ala
NM_172056.2:c.2156G>C , LRG_288t2:c.2156G>C	NP_742053.1:p.Gly719Ala
NM_172057.2:c.1136G>C , LRG_288t3:c.1136G>C	NP_742054.1:p.Gly379Ala
XM_011516185.1:c.1856G>C	XP_011514487.1:p.Gly619Ala
XM_011516186.1:c.2156G>C	XP_011514488.1:p.Gly719Ala
XM_011516185.2:c.1856G>C	XP_011514487.1:p.Gly619Ala
XM_011516186.3:c.2156G>C	XP_011514488.1:p.Gly719Ala
XM_017012195.1:c.2006G>C	XP_016867684.1:p.Gly669Ala
XM_017012196.1:c.1979G>C	XP_016867685.1:p.Gly660Ala
NM_000238.4:c.2156G>C MANE Select	NP_000229.1:p.Gly719Ala
NM_001204798.2:c.1136G>C	NP_001191727.1:p.Gly379Ala
NM_172057.3:c.1136G>C	NP_742054.1:p.Gly379Ala