Canonical Allele Identifier: CA1948243193
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572889_2572892delinsTCTC , CM000673.2:g.2572889_2572892delinsTCTC GRCh38
NC_000011.9:g.2594119_2594122delinsTCTC , CM000673.1:g.2594119_2594122delinsTCTC GRCh37
NC_000011.8:g.2550695_2550698delinsTCTC NCBI36
NG_008935.1:g.132899_132902delinsTCTC , LRG_287:g.132899_132902delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.563_566delinsTCTC ENSP00000434560.2:p.Phe188=
ENST00000646564.2:c.478-10546_478-10543delinsTCTC ENSP00000495806.2:n.478-10546_478-10543de...
ENST00000155840.12:c.824_827delinsTCTC MANE Select ENSP00000155840.2:p.Phe275=
ENST00000335475.6:c.443_446delinsTCTC ENSP00000334497.5:p.Phe148=
ENST00000646564.1:c.124-10546_124-10543delinsTCTC ENSP00000495806.1:n.124-10546_124-10543de...
ENST00000155840.9:c.824_827delinsTCTC ENSP00000155840.2:p.Phe275=
ENST00000335475.5:c.443_446delinsTCTC ENSP00000334497.5:p.Phe148=
ENST00000496887.6:c.563_566delinsTCTC ENSP00000434560.1:p.Phe188=
NM_000218.2:c.824_827delinsTCTC , LRG_287t1:c.824_827delinsTCTC NP_000209.2:p.Phe275=
NM_181798.1:c.443_446delinsTCTC , LRG_287t2:c.443_446delinsTCTC NP_861463.1:p.Phe148=
NM_000218.3:c.824_827delinsTCTC MANE Select NP_000209.2:p.Phe275=