Canonical Allele Identifier: CA458645428

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648129T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951041T>G , CM000669.2:g.150951041T>G	GRCh38
NC_000007.13:g.150648129T>G , CM000669.1:g.150648129T>G	GRCh37
NC_000007.12:g.150279062T>G	NCBI36
NG_008916.1:g.31886A>C , LRG_288:g.31886A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1323A>C
ENST00000683359.1:n.149A>C
ENST00000684241.1:n.2858A>C
ENST00000262186.10:c.2025A>C MANE Select	ENSP00000262186.5:p.Thr675=
ENST00000330883.9:c.1005A>C	ENSP00000328531.4:p.Thr335=
ENST00000262186.9:c.2025A>C	ENSP00000262186.5:p.Thr675=
ENST00000330883.8:c.1005A>C	ENSP00000328531.4:p.Thr335=
ENST00000430723.4:c.1677A>C	ENSP00000387657.4:p.Thr559=
ENST00000461280.1:n.1312A>C
ENST00000473610.5:n.1657A>C
ENST00000532957.5:n.2248A>C
NM_000238.3:c.2025A>C , LRG_288t1:c.2025A>C	NP_000229.1:p.Thr675=
NM_001204798.1:c.1005A>C	NP_001191727.1:p.Thr335=
NM_172056.2:c.2025A>C , LRG_288t2:c.2025A>C	NP_742053.1:p.Thr675=
NM_172057.2:c.1005A>C , LRG_288t3:c.1005A>C	NP_742054.1:p.Thr335=
XM_011516185.1:c.1725A>C	XP_011514487.1:p.Thr575=
XM_011516186.1:c.2025A>C	XP_011514488.1:p.Thr675=
XM_011516185.2:c.1725A>C	XP_011514487.1:p.Thr575=
XM_011516186.3:c.2025A>C	XP_011514488.1:p.Thr675=
XM_017012195.1:c.1875A>C	XP_016867684.1:p.Thr625=
XM_017012196.1:c.1848A>C	XP_016867685.1:p.Thr616=
NM_000238.4:c.2025A>C MANE Select	NP_000229.1:p.Thr675=
NM_001204798.2:c.1005A>C	NP_001191727.1:p.Thr335=
NM_172057.3:c.1005A>C	NP_742054.1:p.Thr335=