Canonical Allele Identifier: CA369860334

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649920C>G (hg19) ; chr7:g.150952832C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952832C>G , CM000669.2:g.150952832C>G	GRCh38
NC_000007.13:g.150649920C>G , CM000669.1:g.150649920C>G	GRCh37
NC_000007.12:g.150280853C>G	NCBI36
NG_008916.1:g.30095G>C , LRG_288:g.30095G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.448G>C
ENST00000684116.1:n.43G>C
ENST00000684241.1:n.1983G>C
ENST00000262186.10:c.1150G>C MANE Select	ENSP00000262186.5:p.Val384Leu
ENST00000330883.9:c.130G>C	ENSP00000328531.4:p.Val44Leu
ENST00000262186.9:c.1150G>C	ENSP00000262186.5:p.Val384Leu
ENST00000330883.8:c.130G>C	ENSP00000328531.4:p.Val44Leu
ENST00000430723.4:c.802G>C	ENSP00000387657.4:p.Val268Leu
ENST00000461280.1:n.437G>C
ENST00000473610.5:n.455G>C
ENST00000532957.5:n.1373G>C
NM_000238.3:c.1150G>C , LRG_288t1:c.1150G>C	NP_000229.1:p.Val384Leu
NM_001204798.1:c.130G>C	NP_001191727.1:p.Val44Leu
NM_172056.2:c.1150G>C , LRG_288t2:c.1150G>C	NP_742053.1:p.Val384Leu
NM_172057.2:c.130G>C , LRG_288t3:c.130G>C	NP_742054.1:p.Val44Leu
XM_011516185.1:c.850G>C	XP_011514487.1:p.Val284Leu
XM_011516186.1:c.1150G>C	XP_011514488.1:p.Val384Leu
XM_011516185.2:c.850G>C	XP_011514487.1:p.Val284Leu
XM_011516186.3:c.1150G>C	XP_011514488.1:p.Val384Leu
XM_017012195.1:c.1000G>C	XP_016867684.1:p.Val334Leu
XM_017012196.1:c.973G>C	XP_016867685.1:p.Val325Leu
NM_000238.4:c.1150G>C MANE Select	NP_000229.1:p.Val384Leu
NM_001204798.2:c.130G>C	NP_001191727.1:p.Val44Leu
NM_172057.3:c.130G>C	NP_742054.1:p.Val44Leu