Canonical Allele Identifier: CA2661696303

Gene: KCNH7

Linked Data

• gnomAD v4: 2-162435120-TTACTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435123_162435127del , CM000664.2:g.162435123_162435127del	GRCh38
NC_000002.11:g.163291633_163291637del , CM000664.1:g.163291633_163291637del	GRCh37
NC_000002.10:g.162999879_162999883del	NCBI36
NG_041938.1:g.408623_408627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1954+73_1954+77del MANE Select	ENSP00000331727.5:n.1954+73_1954+77del
ENST00000328032.8:c.1933+73_1933+77del	ENSP00000333781.4:n.1933+73_1933+77del
ENST00000332142.9:c.1954+73_1954+77del	ENSP00000331727.5:n.1954+73_1954+77del
ENST00000618399.4:c.1654+73_1654+77del	ENSP00000482818.1:n.1654+73_1654+77del
ENST00000621889.1:c.1627+73_1627+77del	ENSP00000483158.1:n.1627+73_1627+77del
NM_033272.3:c.1954+73_1954+77del	NP_150375.2:n.1954+73_1954+77del
NM_173162.2:c.1933+73_1933+77del	NP_775185.1:n.1933+73_1933+77del
XM_011512109.1:c.1978+73_1978+77del	XP_011510411.1:n.1978+73_1978+77del
XM_011512109.3:c.1978+73_1978+77del	XP_011510411.1:n.1978+73_1978+77del
XM_017005218.2:c.1978+73_1978+77del	XP_016860707.1:n.1978+73_1978+77del
XM_017005219.2:c.1954+73_1954+77del	XP_016860708.1:n.1954+73_1954+77del
XM_017005220.2:c.1933+73_1933+77del	XP_016860709.1:n.1933+73_1933+77del
NM_033272.4:c.1954+73_1954+77del MANE Select	NP_150375.2:n.1954+73_1954+77del
NM_173162.3:c.1933+73_1933+77del	NP_775185.1:n.1933+73_1933+77del