Canonical Allele Identifier: CA2612004115
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572825_2572826del , CM000673.2:g.2572825_2572826del GRCh38
NC_000011.9:g.2594055_2594056del , CM000673.1:g.2594055_2594056del GRCh37
NC_000011.8:g.2550631_2550632del NCBI36
NG_008935.1:g.132835_132836del , LRG_287:g.132835_132836del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.520-21_520-20del ENSP00000434560.2:n.520-21_520-20del
ENST00000646564.2:c.478-10610_478-10609del ENSP00000495806.2:n.478-10610_478-10609de...
ENST00000155840.12:c.781-21_781-20del MANE Select ENSP00000155840.2:n.781-21_781-20del
ENST00000335475.6:c.400-21_400-20del ENSP00000334497.5:n.400-21_400-20del
ENST00000646564.1:c.124-10610_124-10609del ENSP00000495806.1:n.124-10610_124-10609de...
ENST00000155840.9:c.781-21_781-20del ENSP00000155840.2:n.781-21_781-20del
ENST00000335475.5:c.400-21_400-20del ENSP00000334497.5:n.400-21_400-20del
ENST00000496887.6:c.520-21_520-20del ENSP00000434560.1:n.520-21_520-20del
NM_000218.2:c.781-21_781-20del , LRG_287t1:c.781-21_781-20del NP_000209.2:n.781-21_781-20del
NM_181798.1:c.400-21_400-20del , LRG_287t2:c.400-21_400-20del NP_861463.1:n.400-21_400-20del
NM_000218.3:c.781-21_781-20del MANE Select NP_000209.2:n.781-21_781-20del