Canonical Allele Identifier: CA458870899

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644956C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947868C>T , CM000669.2:g.150947868C>T	GRCh38
NC_000007.13:g.150644956C>T , CM000669.1:g.150644956C>T	GRCh37
NC_000007.12:g.150275889C>T	NCBI36
NG_008916.1:g.35059G>A , LRG_288:g.35059G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3536G>A
ENST00000262186.10:c.2703G>A MANE Select	ENSP00000262186.5:p.Gln901=
ENST00000330883.9:c.1683G>A	ENSP00000328531.4:p.Gln561=
ENST00000262186.9:c.2703G>A	ENSP00000262186.5:p.Gln901=
ENST00000330883.8:c.1683G>A	ENSP00000328531.4:p.Gln561=
NM_000238.3:c.2703G>A , LRG_288t1:c.2703G>A	NP_000229.1:p.Gln901=
NM_172057.2:c.1683G>A , LRG_288t3:c.1683G>A	NP_742054.1:p.Gln561=
XM_011516185.1:c.2403G>A	XP_011514487.1:p.Gln801=
XM_011516186.1:c.2693-177G>A	XP_011514488.1:n.2693-177G>A
XM_011516185.2:c.2403G>A	XP_011514487.1:p.Gln801=
XM_011516186.3:c.2693-177G>A	XP_011514488.1:n.2693-177G>A
XM_017012195.1:c.2553G>A	XP_016867684.1:p.Gln851=
XM_017012196.1:c.2526G>A	XP_016867685.1:p.Gln842=
NM_000238.4:c.2703G>A MANE Select	NP_000229.1:p.Gln901=
NM_172057.3:c.1683G>A	NP_742054.1:p.Gln561=