Canonical Allele Identifier: CA369852519

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947343-T-A
• MyVariant Identifiers: chr7:g.150644431T>A (hg19) ; chr7:g.150947343T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947343T>A , CM000669.2:g.150947343T>A	GRCh38
NC_000007.13:g.150644431T>A , CM000669.1:g.150644431T>A	GRCh37
NC_000007.12:g.150275364T>A	NCBI36
NG_008916.1:g.35584A>T , LRG_288:g.35584A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3970A>T
ENST00000262186.10:c.3137A>T MANE Select	ENSP00000262186.5:p.Gln1046Leu
ENST00000330883.9:c.2117A>T	ENSP00000328531.4:p.Gln706Leu
ENST00000262186.9:c.3137A>T	ENSP00000262186.5:p.Gln1046Leu
ENST00000330883.8:c.2117A>T	ENSP00000328531.4:p.Gln706Leu
NM_000238.3:c.3137A>T , LRG_288t1:c.3137A>T	NP_000229.1:p.Gln1046Leu
NM_172057.2:c.2117A>T , LRG_288t3:c.2117A>T	NP_742054.1:p.Gln706Leu
XM_011516185.1:c.2837A>T	XP_011514487.1:p.Gln946Leu
XM_011516185.2:c.2837A>T	XP_011514487.1:p.Gln946Leu
XM_017012195.1:c.2987A>T	XP_016867684.1:p.Gln996Leu
XM_017012196.1:c.2960A>T	XP_016867685.1:p.Gln987Leu
NM_000238.4:c.3137A>T MANE Select	NP_000229.1:p.Gln1046Leu
NM_172057.3:c.2117A>T	NP_742054.1:p.Gln706Leu