Canonical Allele Identifier: CA369857726

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648178A>G (hg19) ; chr7:g.150951090A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951090A>G , CM000669.2:g.150951090A>G	GRCh38
NC_000007.13:g.150648178A>G , CM000669.1:g.150648178A>G	GRCh37
NC_000007.12:g.150279111A>G	NCBI36
NG_008916.1:g.31837T>C , LRG_288:g.31837T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1274T>C
ENST00000683359.1:n.100T>C
ENST00000684241.1:n.2809T>C
ENST00000262186.10:c.1976T>C MANE Select	ENSP00000262186.5:p.Val659Ala
ENST00000330883.9:c.956T>C	ENSP00000328531.4:p.Val319Ala
ENST00000262186.9:c.1976T>C	ENSP00000262186.5:p.Val659Ala
ENST00000330883.8:c.956T>C	ENSP00000328531.4:p.Val319Ala
ENST00000430723.4:c.1628T>C	ENSP00000387657.4:p.Val543Ala
ENST00000461280.1:n.1263T>C
ENST00000473610.5:n.1608T>C
ENST00000532957.5:n.2199T>C
NM_000238.3:c.1976T>C , LRG_288t1:c.1976T>C	NP_000229.1:p.Val659Ala
NM_001204798.1:c.956T>C	NP_001191727.1:p.Val319Ala
NM_172056.2:c.1976T>C , LRG_288t2:c.1976T>C	NP_742053.1:p.Val659Ala
NM_172057.2:c.956T>C , LRG_288t3:c.956T>C	NP_742054.1:p.Val319Ala
XM_011516185.1:c.1676T>C	XP_011514487.1:p.Val559Ala
XM_011516186.1:c.1976T>C	XP_011514488.1:p.Val659Ala
XM_011516185.2:c.1676T>C	XP_011514487.1:p.Val559Ala
XM_011516186.3:c.1976T>C	XP_011514488.1:p.Val659Ala
XM_017012195.1:c.1826T>C	XP_016867684.1:p.Val609Ala
XM_017012196.1:c.1799T>C	XP_016867685.1:p.Val600Ala
NM_000238.4:c.1976T>C MANE Select	NP_000229.1:p.Val659Ala
NM_001204798.2:c.956T>C	NP_001191727.1:p.Val319Ala
NM_172057.3:c.956T>C	NP_742054.1:p.Val319Ala