Canonical Allele Identifier: CA2685605965

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150975076-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975076_150975077insT , CM000669.2:g.150975076_150975077insT	GRCh38
NC_000007.13:g.150672164_150672165insT , CM000669.1:g.150672164_150672165insT	GRCh37
NC_000007.12:g.150303097_150303098insT	NCBI36
NG_008916.1:g.7850_7851insA , LRG_288:g.7850_7851insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-136_77-135insA MANE Select	ENSP00000262186.5:n.77-136_77-135insA
ENST00000262186.9:c.77-136_77-135insA	ENSP00000262186.5:n.77-136_77-135insA
ENST00000430723.4:c.-101-136_-101-135insA	ENSP00000387657.4:n.-101-136_-101-135insA
ENST00000532957.5:n.300-136_300-135insA
NM_000238.3:c.77-136_77-135insA , LRG_288t1:c.77-136_77-135insA	NP_000229.1:n.77-136_77-135insA
NM_172056.2:c.77-136_77-135insA , LRG_288t2:c.77-136_77-135insA	NP_742053.1:n.77-136_77-135insA
XM_011516186.1:c.77-136_77-135insA	XP_011514488.1:n.77-136_77-135insA
XM_011516186.3:c.77-136_77-135insA	XP_011514488.1:n.77-136_77-135insA
NM_000238.4:c.77-136_77-135insA MANE Select	NP_000229.1:n.77-136_77-135insA