Canonical Allele Identifier: CA369863750

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656738C>A (hg19) ; chr7:g.150959650C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959650C>A , CM000669.2:g.150959650C>A	GRCh38
NC_000007.13:g.150656738C>A , CM000669.1:g.150656738C>A	GRCh37
NC_000007.12:g.150287671C>A	NCBI36
NG_008916.1:g.23277G>T , LRG_288:g.23277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1227G>T
ENST00000262186.10:c.394G>T MANE Select	ENSP00000262186.5:p.Val132Leu
ENST00000262186.9:c.394G>T	ENSP00000262186.5:p.Val132Leu
ENST00000430723.4:c.217G>T	ENSP00000387657.4:p.Val73Leu
ENST00000532957.5:n.617G>T
NM_000238.3:c.394G>T , LRG_288t1:c.394G>T	NP_000229.1:p.Val132Leu
NM_172056.2:c.394G>T , LRG_288t2:c.394G>T	NP_742053.1:p.Val132Leu
XM_011516185.1:c.94G>T	XP_011514487.1:p.Val32Leu
XM_011516186.1:c.394G>T	XP_011514488.1:p.Val132Leu
XM_011516185.2:c.94G>T	XP_011514487.1:p.Val32Leu
XM_011516186.3:c.394G>T	XP_011514488.1:p.Val132Leu
XM_017012195.1:c.244G>T	XP_016867684.1:p.Val82Leu
XM_017012196.1:c.217G>T	XP_016867685.1:p.Val73Leu
NM_000238.4:c.394G>T MANE Select	NP_000229.1:p.Val132Leu