Canonical Allele Identifier: CA369852785

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947421-G-T
• MyVariant Identifiers: chr7:g.150644509G>T (hg19) ; chr7:g.150947421G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947421G>T , CM000669.2:g.150947421G>T	GRCh38
NC_000007.13:g.150644509G>T , CM000669.1:g.150644509G>T	GRCh37
NC_000007.12:g.150275442G>T	NCBI36
NG_008916.1:g.35506C>A , LRG_288:g.35506C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3892C>A
ENST00000262186.10:c.3059C>A MANE Select	ENSP00000262186.5:p.Pro1020His
ENST00000330883.9:c.2039C>A	ENSP00000328531.4:p.Pro680His
ENST00000262186.9:c.3059C>A	ENSP00000262186.5:p.Pro1020His
ENST00000330883.8:c.2039C>A	ENSP00000328531.4:p.Pro680His
NM_000238.3:c.3059C>A , LRG_288t1:c.3059C>A	NP_000229.1:p.Pro1020His
NM_172057.2:c.2039C>A , LRG_288t3:c.2039C>A	NP_742054.1:p.Pro680His
XM_011516185.1:c.2759C>A	XP_011514487.1:p.Pro920His
XM_011516185.2:c.2759C>A	XP_011514487.1:p.Pro920His
XM_017012195.1:c.2909C>A	XP_016867684.1:p.Pro970His
XM_017012196.1:c.2882C>A	XP_016867685.1:p.Pro961His
NM_000238.4:c.3059C>A MANE Select	NP_000229.1:p.Pro1020His
NM_172057.3:c.2039C>A	NP_742054.1:p.Pro680His