Canonical Allele Identifier: CA369863040

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655432C>G (hg19) ; chr7:g.150958344C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958344C>G , CM000669.2:g.150958344C>G	GRCh38
NC_000007.13:g.150655432C>G , CM000669.1:g.150655432C>G	GRCh37
NC_000007.12:g.150286365C>G	NCBI36
NG_008916.1:g.24583G>C , LRG_288:g.24583G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1464G>C
ENST00000262186.10:c.631G>C MANE Select	ENSP00000262186.5:p.Ala211Pro
ENST00000262186.9:c.631G>C	ENSP00000262186.5:p.Ala211Pro
ENST00000430723.4:c.283G>C	ENSP00000387657.4:p.Ala95Pro
ENST00000532957.5:n.854G>C
NM_000238.3:c.631G>C , LRG_288t1:c.631G>C	NP_000229.1:p.Ala211Pro
NM_172056.2:c.631G>C , LRG_288t2:c.631G>C	NP_742053.1:p.Ala211Pro
XM_011516185.1:c.331G>C	XP_011514487.1:p.Ala111Pro
XM_011516186.1:c.631G>C	XP_011514488.1:p.Ala211Pro
XM_011516185.2:c.331G>C	XP_011514487.1:p.Ala111Pro
XM_011516186.3:c.631G>C	XP_011514488.1:p.Ala211Pro
XM_017012195.1:c.481G>C	XP_016867684.1:p.Ala161Pro
XM_017012196.1:c.454G>C	XP_016867685.1:p.Ala152Pro
NM_000238.4:c.631G>C MANE Select	NP_000229.1:p.Ala211Pro