Canonical Allele Identifier: CA2685610324

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150959778-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959778T>A , CM000669.2:g.150959778T>A	GRCh38
NC_000007.13:g.150656866T>A , CM000669.1:g.150656866T>A	GRCh37
NC_000007.12:g.150287799T>A	NCBI36
NG_008916.1:g.23149A>T , LRG_288:g.23149A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1099A>T
ENST00000262186.10:c.308-42A>T MANE Select	ENSP00000262186.5:n.308-42A>T
ENST00000262186.9:c.308-42A>T	ENSP00000262186.5:n.308-42A>T
ENST00000430723.4:c.131-42A>T	ENSP00000387657.4:n.131-42A>T
ENST00000532957.5:n.531-42A>T
NM_000238.3:c.308-42A>T , LRG_288t1:c.308-42A>T	NP_000229.1:n.308-42A>T
NM_172056.2:c.308-42A>T , LRG_288t2:c.308-42A>T	NP_742053.1:n.308-42A>T
XM_011516185.1:c.8-42A>T	XP_011514487.1:n.8-42A>T
XM_011516186.1:c.308-42A>T	XP_011514488.1:n.308-42A>T
XM_011516185.2:c.8-42A>T	XP_011514487.1:n.8-42A>T
XM_011516186.3:c.308-42A>T	XP_011514488.1:n.308-42A>T
XM_017012195.1:c.158-42A>T	XP_016867684.1:n.158-42A>T
XM_017012196.1:c.131-42A>T	XP_016867685.1:n.131-42A>T
NM_000238.4:c.308-42A>T MANE Select	NP_000229.1:n.308-42A>T