Canonical Allele Identifier: CA369860234

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649872T>G (hg19) ; chr7:g.150952784T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952784T>G , CM000669.2:g.150952784T>G	GRCh38
NC_000007.13:g.150649872T>G , CM000669.1:g.150649872T>G	GRCh37
NC_000007.12:g.150280805T>G	NCBI36
NG_008916.1:g.30143A>C , LRG_288:g.30143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.496A>C
ENST00000684116.1:n.91A>C
ENST00000684241.1:n.2031A>C
ENST00000262186.10:c.1198A>C MANE Select	ENSP00000262186.5:p.Ile400Leu
ENST00000330883.9:c.178A>C	ENSP00000328531.4:p.Ile60Leu
ENST00000262186.9:c.1198A>C	ENSP00000262186.5:p.Ile400Leu
ENST00000330883.8:c.178A>C	ENSP00000328531.4:p.Ile60Leu
ENST00000430723.4:c.850A>C	ENSP00000387657.4:p.Ile284Leu
ENST00000461280.1:n.485A>C
ENST00000473610.5:n.503A>C
ENST00000532957.5:n.1421A>C
NM_000238.3:c.1198A>C , LRG_288t1:c.1198A>C	NP_000229.1:p.Ile400Leu
NM_001204798.1:c.178A>C	NP_001191727.1:p.Ile60Leu
NM_172056.2:c.1198A>C , LRG_288t2:c.1198A>C	NP_742053.1:p.Ile400Leu
NM_172057.2:c.178A>C , LRG_288t3:c.178A>C	NP_742054.1:p.Ile60Leu
XM_011516185.1:c.898A>C	XP_011514487.1:p.Ile300Leu
XM_011516186.1:c.1198A>C	XP_011514488.1:p.Ile400Leu
XM_011516185.2:c.898A>C	XP_011514487.1:p.Ile300Leu
XM_011516186.3:c.1198A>C	XP_011514488.1:p.Ile400Leu
XM_017012195.1:c.1048A>C	XP_016867684.1:p.Ile350Leu
XM_017012196.1:c.1021A>C	XP_016867685.1:p.Ile341Leu
NM_000238.4:c.1198A>C MANE Select	NP_000229.1:p.Ile400Leu
NM_001204798.2:c.178A>C	NP_001191727.1:p.Ile60Leu
NM_172057.3:c.178A>C	NP_742054.1:p.Ile60Leu