Canonical Allele Identifier: CA369855207

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646078C>A (hg19) ; chr7:g.150948990C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948990C>A , CM000669.2:g.150948990C>A	GRCh38
NC_000007.13:g.150646078C>A , CM000669.1:g.150646078C>A	GRCh37
NC_000007.12:g.150277011C>A	NCBI36
NG_008916.1:g.33937G>T , LRG_288:g.33937G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3291G>T
ENST00000262186.10:c.2458G>T MANE Select	ENSP00000262186.5:p.Gly820Trp
ENST00000330883.9:c.1438G>T	ENSP00000328531.4:p.Gly480Trp
ENST00000262186.9:c.2458G>T	ENSP00000262186.5:p.Gly820Trp
ENST00000330883.8:c.1438G>T	ENSP00000328531.4:p.Gly480Trp
NM_000238.3:c.2458G>T , LRG_288t1:c.2458G>T	NP_000229.1:p.Gly820Trp
NM_172057.2:c.1438G>T , LRG_288t3:c.1438G>T	NP_742054.1:p.Gly480Trp
XM_011516185.1:c.2158G>T	XP_011514487.1:p.Gly720Trp
XM_011516186.1:c.2458G>T	XP_011514488.1:p.Gly820Trp
XM_011516185.2:c.2158G>T	XP_011514487.1:p.Gly720Trp
XM_011516186.3:c.2458G>T	XP_011514488.1:p.Gly820Trp
XM_017012195.1:c.2308G>T	XP_016867684.1:p.Gly770Trp
XM_017012196.1:c.2281G>T	XP_016867685.1:p.Gly761Trp
NM_000238.4:c.2458G>T MANE Select	NP_000229.1:p.Gly820Trp
NM_172057.3:c.1438G>T	NP_742054.1:p.Gly480Trp