Canonical Allele Identifier: CA2685602201

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947937-GGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947940_150947942del , CM000669.2:g.150947940_150947942del	GRCh38
NC_000007.13:g.150645028_150645030del , CM000669.1:g.150645028_150645030del	GRCh37
NC_000007.12:g.150275961_150275963del	NCBI36
NG_008916.1:g.34987_34989del , LRG_288:g.34987_34989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3526-62_3526-60del
ENST00000262186.10:c.2693-62_2693-60del MANE Select	ENSP00000262186.5:n.2693-62_2693-60del
ENST00000330883.9:c.1673-62_1673-60del	ENSP00000328531.4:n.1673-62_1673-60del
ENST00000262186.9:c.2693-62_2693-60del	ENSP00000262186.5:n.2693-62_2693-60del
ENST00000330883.8:c.1673-62_1673-60del	ENSP00000328531.4:n.1673-62_1673-60del
NM_000238.3:c.2693-62_2693-60del , LRG_288t1:c.2693-62_2693-60del	NP_000229.1:n.2693-62_2693-60del
NM_172057.2:c.1673-62_1673-60del , LRG_288t3:c.1673-62_1673-60del	NP_742054.1:n.1673-62_1673-60del
XM_011516185.1:c.2393-62_2393-60del	XP_011514487.1:n.2393-62_2393-60del
XM_011516186.1:c.2693-249_2693-247del	XP_011514488.1:n.2693-249_2693-247del
XM_011516185.2:c.2393-62_2393-60del	XP_011514487.1:n.2393-62_2393-60del
XM_011516186.3:c.2693-249_2693-247del	XP_011514488.1:n.2693-249_2693-247del
XM_017012195.1:c.2543-62_2543-60del	XP_016867684.1:n.2543-62_2543-60del
XM_017012196.1:c.2516-62_2516-60del	XP_016867685.1:n.2516-62_2516-60del
NM_000238.4:c.2693-62_2693-60del MANE Select	NP_000229.1:n.2693-62_2693-60del
NM_172057.3:c.1673-62_1673-60del	NP_742054.1:n.1673-62_1673-60del