Canonical Allele Identifier: CA369851408

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150945402-T-C
• MyVariant Identifiers: chr7:g.150642490T>C (hg19) ; chr7:g.150945402T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150945402T>C , CM000669.2:g.150945402T>C	GRCh38
NC_000007.13:g.150642490T>C , CM000669.1:g.150642490T>C	GRCh37
NC_000007.12:g.150273423T>C	NCBI36
NG_008916.1:g.37525A>G , LRG_288:g.37525A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.4276A>G
ENST00000262186.10:c.3443A>G MANE Select	ENSP00000262186.5:p.Gln1148Arg
ENST00000330883.9:c.2423A>G	ENSP00000328531.4:p.Gln808Arg
ENST00000262186.9:c.3443A>G	ENSP00000262186.5:p.Gln1148Arg
ENST00000330883.8:c.2423A>G	ENSP00000328531.4:p.Gln808Arg
NM_000238.3:c.3443A>G , LRG_288t1:c.3443A>G	NP_000229.1:p.Gln1148Arg
NM_172057.2:c.2423A>G , LRG_288t3:c.2423A>G	NP_742054.1:p.Gln808Arg
XM_011516185.1:c.3143A>G	XP_011514487.1:p.Gln1048Arg
XM_011516185.2:c.3143A>G	XP_011514487.1:p.Gln1048Arg
XM_017012195.1:c.3293A>G	XP_016867684.1:p.Gln1098Arg
XM_017012196.1:c.3266A>G	XP_016867685.1:p.Gln1089Arg
NM_000238.4:c.3443A>G MANE Select	NP_000229.1:p.Gln1148Arg
NM_172057.3:c.2423A>G	NP_742054.1:p.Gln808Arg