Canonical Allele Identifier: CA2685602458

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948401-ACCTTGTCCCCGCCCTCCCCCTTCCTCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948405_150948431del , CM000669.2:g.150948405_150948431del	GRCh38
NC_000007.13:g.150645493_150645519del , CM000669.1:g.150645493_150645519del	GRCh37
NC_000007.12:g.150276426_150276452del	NCBI36
NG_008916.1:g.34499_34525del , LRG_288:g.34499_34525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3525+16_3525+42del
ENST00000262186.10:c.2692+16_2692+42del MANE Select	ENSP00000262186.5:n.2692+16_2692+42del
ENST00000330883.9:c.1672+16_1672+42del	ENSP00000328531.4:n.1672+16_1672+42del
ENST00000262186.9:c.2692+16_2692+42del	ENSP00000262186.5:n.2692+16_2692+42del
ENST00000330883.8:c.1672+16_1672+42del	ENSP00000328531.4:n.1672+16_1672+42del
NM_000238.3:c.2692+16_2692+42del , LRG_288t1:c.2692+16_2692+42del	NP_000229.1:n.2692+16_2692+42del
NM_172057.2:c.1672+16_1672+42del , LRG_288t3:c.1672+16_1672+42del	NP_742054.1:n.1672+16_1672+42del
XM_011516185.1:c.2392+16_2392+42del	XP_011514487.1:n.2392+16_2392+42del
XM_011516186.1:c.2692+16_2692+42del	XP_011514488.1:n.2692+16_2692+42del
XM_011516185.2:c.2392+16_2392+42del	XP_011514487.1:n.2392+16_2392+42del
XM_011516186.3:c.2692+16_2692+42del	XP_011514488.1:n.2692+16_2692+42del
XM_017012195.1:c.2542+16_2542+42del	XP_016867684.1:n.2542+16_2542+42del
XM_017012196.1:c.2515+16_2515+42del	XP_016867685.1:n.2515+16_2515+42del
NM_000238.4:c.2692+16_2692+42del MANE Select	NP_000229.1:n.2692+16_2692+42del
NM_172057.3:c.1672+16_1672+42del	NP_742054.1:n.1672+16_1672+42del