Canonical Allele Identifier: CA1303193955

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162381069_162381071delinsCTG , CM000664.2:g.162381069_162381071delinsCTG	GRCh38
NC_000002.11:g.163237579_163237581delinsCTG , CM000664.1:g.163237579_163237581delinsCTG	GRCh37
NC_000002.10:g.162945825_162945827delinsCTG	NCBI36
NG_041938.1:g.462677_462679delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.2963-1050_2963-1048delinsCAG MANE Select	ENSP00000331727.5:n.2963-1050_2963-1048delinsCAG
ENST00000332142.9:c.2963-1050_2963-1048delinsCAG	ENSP00000331727.5:n.2963-1050_2963-1048delinsCAG
ENST00000618399.4:c.2663-1050_2663-1048delinsCAG	ENSP00000482818.1:n.2663-1050_2663-1048delinsCAG
NM_033272.3:c.2963-1050_2963-1048delinsCAG	NP_150375.2:n.2963-1050_2963-1048delinsCAG
XM_011512109.1:c.2987-1050_2987-1048delinsCAG	XP_011510411.1:n.2987-1050_2987-1048delinsCAG
XM_011512109.3:c.2987-1050_2987-1048delinsCAG	XP_011510411.1:n.2987-1050_2987-1048delinsCAG
XM_017005218.2:c.2978-1050_2978-1048delinsCAG	XP_016860707.1:n.2978-1050_2978-1048delinsCAG
XM_017005219.2:c.2954-1050_2954-1048delinsCAG	XP_016860708.1:n.2954-1050_2954-1048delinsCAG
XM_017005220.2:c.2942-1050_2942-1048delinsCAG	XP_016860709.1:n.2942-1050_2942-1048delinsCAG
NM_033272.4:c.2963-1050_2963-1048delinsCAG MANE Select	NP_150375.2:n.2963-1050_2963-1048delinsCAG