Canonical Allele Identifier: CA1303193913

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162380978_162380979delinsAT , CM000664.2:g.162380978_162380979delinsAT	GRCh38
NC_000002.11:g.163237488_163237489delinsAT , CM000664.1:g.163237488_163237489delinsAT	GRCh37
NC_000002.10:g.162945734_162945735delinsAT	NCBI36
NG_041938.1:g.462769_462770delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-958_2963-957delinsAT MANE Select	ENSP00000331727.5:n.2963-958_2963-957delinsAT
ENST00000332142.9:c.2963-958_2963-957delinsAT	ENSP00000331727.5:n.2963-958_2963-957delinsAT
ENST00000618399.4:c.2663-958_2663-957delinsAT	ENSP00000482818.1:n.2663-958_2663-957delinsAT
NM_033272.3:c.2963-958_2963-957delinsAT	NP_150375.2:n.2963-958_2963-957delinsAT
XM_011512109.1:c.2987-958_2987-957delinsAT	XP_011510411.1:n.2987-958_2987-957delinsAT
XM_011512109.3:c.2987-958_2987-957delinsAT	XP_011510411.1:n.2987-958_2987-957delinsAT
XM_017005218.2:c.2978-958_2978-957delinsAT	XP_016860707.1:n.2978-958_2978-957delinsAT
XM_017005219.2:c.2954-958_2954-957delinsAT	XP_016860708.1:n.2954-958_2954-957delinsAT
XM_017005220.2:c.2942-958_2942-957delinsAT	XP_016860709.1:n.2942-958_2942-957delinsAT
NM_033272.4:c.2963-958_2963-957delinsAT MANE Select	NP_150375.2:n.2963-958_2963-957delinsAT