Canonical Allele Identifier: CA2685601940

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947425-T-TTTGTGGCGGTGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947425_150947426insTTGTGGCGGTGGGGGGGGGG , CM000669.2:g.150947425_150947426insTTGTGGCGGTGGGGGGGGGG	GRCh38
NC_000007.13:g.150644513_150644514insTTGTGGCGGTGGGGGGGGGG , CM000669.1:g.150644513_150644514insTTGTGGCGGTGGGGGGGGGG	GRCh37
NC_000007.12:g.150275446_150275447insTTGTGGCGGTGGGGGGGGGG	NCBI36
NG_008916.1:g.35501_35502insCCCCCCCCCCACCGCCACAA , LRG_288:g.35501_35502insCCCCCCCCCCACCGCCACAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3887_3888insCCCCCCCCCCACCGCCACAA
ENST00000262186.10:c.3054_3055insCCCCCCCCCCACCGCCACAA MANE Select	ENSP00000262186.5:p.Thr1019ProfsTer?
ENST00000330883.9:c.2034_2035insCCCCCCCCCCACCGCCACAA	ENSP00000328531.4:p.Thr679ProfsTer?
ENST00000262186.9:c.3054_3055insCCCCCCCCCCACCGCCACAA	ENSP00000262186.5:p.Thr1019ProfsTer?
ENST00000330883.8:c.2034_2035insCCCCCCCCCCACCGCCACAA	ENSP00000328531.4:p.Thr679ProfsTer?
NM_000238.3:c.3054_3055insCCCCCCCCCCACCGCCACAA , LRG_288t1:c.3054_3055insCCCCCCCCCCACCGCCACAA	NP_000229.1:p.Thr1019ProfsTer?
NM_172057.2:c.2034_2035insCCCCCCCCCCACCGCCACAA , LRG_288t3:c.2034_2035insCCCCCCCCCCACCGCCACAA	NP_742054.1:p.Thr679ProfsTer?
XM_011516185.1:c.2754_2755insCCCCCCCCCCACCGCCACAA	XP_011514487.1:p.Thr919ProfsTer?
XM_011516186.1:c.*134_*135insCCCCCCCCCCACCGCCACAA	XP_011514488.1:n.*134_*135insCCCCCCCCCCACCGCCACAA
XM_011516185.2:c.2754_2755insCCCCCCCCCCACCGCCACAA	XP_011514487.1:p.Thr919ProfsTer?
XM_011516186.3:c.*134_*135insCCCCCCCCCCACCGCCACAA	XP_011514488.1:n.*134_*135insCCCCCCCCCCACCGCCACAA
XM_017012195.1:c.2904_2905insCCCCCCCCCCACCGCCACAA	XP_016867684.1:p.Thr969ProfsTer?
XM_017012196.1:c.2877_2878insCCCCCCCCCCACCGCCACAA	XP_016867685.1:p.Thr960ProfsTer?
NM_000238.4:c.3054_3055insCCCCCCCCCCACCGCCACAA MANE Select	NP_000229.1:p.Thr1019ProfsTer?
NM_172057.3:c.2034_2035insCCCCCCCCCCACCGCCACAA	NP_742054.1:p.Thr679ProfsTer?