Canonical Allele Identifier: CA1303193936

Gene: KCNH7

Linked Data

• dbSNP Id: rs1686400194

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162381031_162381033del , CM000664.2:g.162381031_162381033del	GRCh38
NC_000002.11:g.163237541_163237543del , CM000664.1:g.163237541_163237543del	GRCh37
NC_000002.10:g.162945787_162945789del	NCBI36
NG_041938.1:g.462716_462718del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-1011_2963-1009del MANE Select	ENSP00000331727.5:n.2963-1011_2963-1009del
ENST00000332142.9:c.2963-1011_2963-1009del	ENSP00000331727.5:n.2963-1011_2963-1009del
ENST00000618399.4:c.2663-1011_2663-1009del	ENSP00000482818.1:n.2663-1011_2663-1009del
NM_033272.3:c.2963-1011_2963-1009del	NP_150375.2:n.2963-1011_2963-1009del
XM_011512109.1:c.2987-1011_2987-1009del	XP_011510411.1:n.2987-1011_2987-1009del
XM_011512109.3:c.2987-1011_2987-1009del	XP_011510411.1:n.2987-1011_2987-1009del
XM_017005218.2:c.2978-1011_2978-1009del	XP_016860707.1:n.2978-1011_2978-1009del
XM_017005219.2:c.2954-1011_2954-1009del	XP_016860708.1:n.2954-1011_2954-1009del
XM_017005220.2:c.2942-1011_2942-1009del	XP_016860709.1:n.2942-1011_2942-1009del
NM_033272.4:c.2963-1011_2963-1009del MANE Select	NP_150375.2:n.2963-1011_2963-1009del