Canonical Allele Identifier: CA369861680

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654507G>T (hg19) ; chr7:g.150957419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957419G>T , CM000669.2:g.150957419G>T	GRCh38
NC_000007.13:g.150654507G>T , CM000669.1:g.150654507G>T	GRCh37
NC_000007.12:g.150285440G>T	NCBI36
NG_008916.1:g.25508C>A , LRG_288:g.25508C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1833C>A
ENST00000262186.10:c.1000C>A MANE Select	ENSP00000262186.5:p.Pro334Thr
ENST00000262186.9:c.1000C>A	ENSP00000262186.5:p.Pro334Thr
ENST00000430723.4:c.652C>A	ENSP00000387657.4:p.Pro218Thr
ENST00000532957.5:n.1223C>A
NM_000238.3:c.1000C>A , LRG_288t1:c.1000C>A	NP_000229.1:p.Pro334Thr
NM_172056.2:c.1000C>A , LRG_288t2:c.1000C>A	NP_742053.1:p.Pro334Thr
XM_011516185.1:c.700C>A	XP_011514487.1:p.Pro234Thr
XM_011516186.1:c.1000C>A	XP_011514488.1:p.Pro334Thr
XM_011516185.2:c.700C>A	XP_011514487.1:p.Pro234Thr
XM_011516186.3:c.1000C>A	XP_011514488.1:p.Pro334Thr
XM_017012195.1:c.850C>A	XP_016867684.1:p.Pro284Thr
XM_017012196.1:c.823C>A	XP_016867685.1:p.Pro275Thr
NM_000238.4:c.1000C>A MANE Select	NP_000229.1:p.Pro334Thr