Canonical Allele Identifier: CA369859691

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649599C>G (hg19) ; chr7:g.150952511C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952511C>G , CM000669.2:g.150952511C>G	GRCh38
NC_000007.13:g.150649599C>G , CM000669.1:g.150649599C>G	GRCh37
NC_000007.12:g.150280532C>G	NCBI36
NG_008916.1:g.30416G>C , LRG_288:g.30416G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.769G>C
ENST00000684116.1:n.364G>C
ENST00000684241.1:n.2304G>C
ENST00000262186.10:c.1471G>C MANE Select	ENSP00000262186.5:p.Val491Leu
ENST00000330883.9:c.451G>C	ENSP00000328531.4:p.Val151Leu
ENST00000262186.9:c.1471G>C	ENSP00000262186.5:p.Val491Leu
ENST00000330883.8:c.451G>C	ENSP00000328531.4:p.Val151Leu
ENST00000430723.4:c.1123G>C	ENSP00000387657.4:p.Val375Leu
ENST00000461280.1:n.758G>C
ENST00000473610.5:n.776G>C
ENST00000532957.5:n.1694G>C
NM_000238.3:c.1471G>C , LRG_288t1:c.1471G>C	NP_000229.1:p.Val491Leu
NM_001204798.1:c.451G>C	NP_001191727.1:p.Val151Leu
NM_172056.2:c.1471G>C , LRG_288t2:c.1471G>C	NP_742053.1:p.Val491Leu
NM_172057.2:c.451G>C , LRG_288t3:c.451G>C	NP_742054.1:p.Val151Leu
XM_011516185.1:c.1171G>C	XP_011514487.1:p.Val391Leu
XM_011516186.1:c.1471G>C	XP_011514488.1:p.Val491Leu
XM_011516185.2:c.1171G>C	XP_011514487.1:p.Val391Leu
XM_011516186.3:c.1471G>C	XP_011514488.1:p.Val491Leu
XM_017012195.1:c.1321G>C	XP_016867684.1:p.Val441Leu
XM_017012196.1:c.1294G>C	XP_016867685.1:p.Val432Leu
NM_000238.4:c.1471G>C MANE Select	NP_000229.1:p.Val491Leu
NM_001204798.2:c.451G>C	NP_001191727.1:p.Val151Leu
NM_172057.3:c.451G>C	NP_742054.1:p.Val151Leu