Canonical Allele Identifier: CA2778426139

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958649_150958659del , CM000669.2:g.150958649_150958659del	GRCh38
NC_000007.13:g.150655737_150655747del , CM000669.1:g.150655737_150655747del	GRCh37
NC_000007.12:g.150286670_150286680del	NCBI36
NG_008916.1:g.24268_24278del , LRG_288:g.24268_24278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1306-157_1306-147del
ENST00000262186.10:c.473-157_473-147del MANE Select	ENSP00000262186.5:n.473-157_473-147del
ENST00000262186.9:c.473-157_473-147del	ENSP00000262186.5:n.473-157_473-147del
ENST00000430723.4:c.235-267_235-257del	ENSP00000387657.4:n.235-267_235-257del
ENST00000532957.5:n.696-157_696-147del
NM_000238.3:c.473-157_473-147del , LRG_288t1:c.473-157_473-147del	NP_000229.1:n.473-157_473-147del
NM_172056.2:c.473-157_473-147del , LRG_288t2:c.473-157_473-147del	NP_742053.1:n.473-157_473-147del
XM_011516185.1:c.173-157_173-147del	XP_011514487.1:n.173-157_173-147del
XM_011516186.1:c.473-157_473-147del	XP_011514488.1:n.473-157_473-147del
XM_011516185.2:c.173-157_173-147del	XP_011514487.1:n.173-157_173-147del
XM_011516186.3:c.473-157_473-147del	XP_011514488.1:n.473-157_473-147del
XM_017012195.1:c.323-157_323-147del	XP_016867684.1:n.323-157_323-147del
XM_017012196.1:c.296-157_296-147del	XP_016867685.1:n.296-157_296-147del
NM_000238.4:c.473-157_473-147del MANE Select	NP_000229.1:n.473-157_473-147del