Canonical Allele Identifier: CA1303193969

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162381088_162381090delinsTTG , CM000664.2:g.162381088_162381090delinsTTG	GRCh38
NC_000002.11:g.163237598_163237600delinsTTG , CM000664.1:g.163237598_163237600delinsTTG	GRCh37
NC_000002.10:g.162945844_162945846delinsTTG	NCBI36
NG_041938.1:g.462658_462660delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-1069_2963-1067delinsCAA MANE Select	ENSP00000331727.5:n.2963-1069_2963-1067delinsCAA
ENST00000332142.9:c.2963-1069_2963-1067delinsCAA	ENSP00000331727.5:n.2963-1069_2963-1067delinsCAA
ENST00000618399.4:c.2663-1069_2663-1067delinsCAA	ENSP00000482818.1:n.2663-1069_2663-1067delinsCAA
NM_033272.3:c.2963-1069_2963-1067delinsCAA	NP_150375.2:n.2963-1069_2963-1067delinsCAA
XM_011512109.1:c.2987-1069_2987-1067delinsCAA	XP_011510411.1:n.2987-1069_2987-1067delinsCAA
XM_011512109.3:c.2987-1069_2987-1067delinsCAA	XP_011510411.1:n.2987-1069_2987-1067delinsCAA
XM_017005218.2:c.2978-1069_2978-1067delinsCAA	XP_016860707.1:n.2978-1069_2978-1067delinsCAA
XM_017005219.2:c.2954-1069_2954-1067delinsCAA	XP_016860708.1:n.2954-1069_2954-1067delinsCAA
XM_017005220.2:c.2942-1069_2942-1067delinsCAA	XP_016860709.1:n.2942-1069_2942-1067delinsCAA
NM_033272.4:c.2963-1069_2963-1067delinsCAA MANE Select	NP_150375.2:n.2963-1069_2963-1067delinsCAA