Canonical Allele Identifier: CA1303193943

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162381040_162381041delinsTG , CM000664.2:g.162381040_162381041delinsTG	GRCh38
NC_000002.11:g.163237550_163237551delinsTG , CM000664.1:g.163237550_163237551delinsTG	GRCh37
NC_000002.10:g.162945796_162945797delinsTG	NCBI36
NG_041938.1:g.462707_462708delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-1020_2963-1019delinsCA MANE Select	ENSP00000331727.5:n.2963-1020_2963-1019delinsCA
ENST00000332142.9:c.2963-1020_2963-1019delinsCA	ENSP00000331727.5:n.2963-1020_2963-1019delinsCA
ENST00000618399.4:c.2663-1020_2663-1019delinsCA	ENSP00000482818.1:n.2663-1020_2663-1019delinsCA
NM_033272.3:c.2963-1020_2963-1019delinsCA	NP_150375.2:n.2963-1020_2963-1019delinsCA
XM_011512109.1:c.2987-1020_2987-1019delinsCA	XP_011510411.1:n.2987-1020_2987-1019delinsCA
XM_011512109.3:c.2987-1020_2987-1019delinsCA	XP_011510411.1:n.2987-1020_2987-1019delinsCA
XM_017005218.2:c.2978-1020_2978-1019delinsCA	XP_016860707.1:n.2978-1020_2978-1019delinsCA
XM_017005219.2:c.2954-1020_2954-1019delinsCA	XP_016860708.1:n.2954-1020_2954-1019delinsCA
XM_017005220.2:c.2942-1020_2942-1019delinsCA	XP_016860709.1:n.2942-1020_2942-1019delinsCA
NM_033272.4:c.2963-1020_2963-1019delinsCA MANE Select	NP_150375.2:n.2963-1020_2963-1019delinsCA