Canonical Allele Identifier: CA369865998

Gene: KCNH2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974926A>T , CM000669.2:g.150974926A>T	GRCh38
NC_000007.13:g.150672014A>T , CM000669.1:g.150672014A>T	GRCh37
NC_000007.12:g.150302947A>T	NCBI36
NG_008916.1:g.8001T>A , LRG_288:g.8001T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.92T>A MANE Select	ENSP00000262186.5:p.Ile31Asn
ENST00000262186.9:c.92T>A	ENSP00000262186.5:p.Ile31Asn
ENST00000430723.4:c.-86T>A	ENSP00000387657.4:n.-86T>A
ENST00000532957.5:n.315T>A
NM_000238.3:c.92T>A , LRG_288t1:c.92T>A	NP_000229.1:p.Ile31Asn
NM_172056.2:c.92T>A , LRG_288t2:c.92T>A	NP_742053.1:p.Ile31Asn
XM_011516186.1:c.92T>A	XP_011514488.1:p.Ile31Asn
XM_011516186.3:c.92T>A	XP_011514488.1:p.Ile31Asn
XM_017012196.1:c.-86T>A	XP_016867685.1:n.-86T>A
NM_000238.4:c.92T>A MANE Select	NP_000229.1:p.Ile31Asn