Canonical Allele Identifier: CA1108704886

Gene: KCNH2

Linked Data

• gnomAD v3: 7-150948407-T-TCCCCCCCCCCCCCCCTCCCCCCCC
• gnomAD v4: 7-150948407-T-TCCCCCCCCCCCCCCCTCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948411_150948412insCCCCCCCCCCCTCCCCCCCCCCCC , CM000669.2:g.150948411_150948412insCCCCCCCCCCCTCCCCCCCCCCCC	GRCh38
NC_000007.13:g.150645499_150645500insCCCCCCCCCCCTCCCCCCCCCCCC , CM000669.1:g.150645499_150645500insCCCCCCCCCCCTCCCCCCCCCCCC	GRCh37
NC_000007.12:g.150276432_150276433insCCCCCCCCCCCTCCCCCCCCCCCC	NCBI36
NG_008916.1:g.34519_34520insGGGGGGGGAGGGGGGGGGGGGGGG , LRG_288:g.34519_34520insGGGGGGGGAGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3525+36_3525+37insGGGGGGGGAGGGGGGGGGGGGGGG
ENST00000262186.10:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG MANE Select	ENSP00000262186.5:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGG...
ENST00000330883.9:c.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG	ENSP00000328531.4:n.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGG...
ENST00000262186.9:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG	ENSP00000262186.5:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGG...
ENST00000330883.8:c.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG	ENSP00000328531.4:n.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGG...
NM_000238.3:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG , LRG_288t1:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG	NP_000229.1:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG
NM_172057.2:c.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG , LRG_288t3:c.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG	NP_742054.1:n.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_011516185.1:c.2392+36_2392+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_011514487.1:n.2392+36_2392+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_011516186.1:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_011514488.1:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_011516185.2:c.2392+36_2392+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_011514487.1:n.2392+36_2392+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_011516186.3:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_011514488.1:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_017012195.1:c.2542+36_2542+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_016867684.1:n.2542+36_2542+37insGGGGGGGGAGGGGGGGGGGGGGGG
XM_017012196.1:c.2515+36_2515+37insGGGGGGGGAGGGGGGGGGGGGGGG	XP_016867685.1:n.2515+36_2515+37insGGGGGGGGAGGGGGGGGGGGGGGG
NM_000238.4:c.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG MANE Select	NP_000229.1:n.2692+36_2692+37insGGGGGGGGAGGGGGGGGGGGGGGG
NM_172057.3:c.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG	NP_742054.1:n.1672+36_1672+37insGGGGGGGGAGGGGGGGGGGGGGGG