Canonical Allele Identifier: CA1948350318
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2849061_2849076delinsTGCAGTTCCCCTGGAA , CM000673.2:g.2849061_2849076delinsTGCAGTTCCCCTGGAA GRCh38
NC_000011.9:g.2870291_2870306delinsTGCAGTTCCCCTGGAA , CM000673.1:g.2870291_2870306delinsTGCAGTTCCCCTGGAA GRCh37
NC_000011.8:g.2826867_2826882delinsTGCAGTTCCCCTGGAA NCBI36
NG_008935.1:g.409071_409086delinsTGCAGTTCCCCTGGAA , LRG_287:g.409071_409086delinsTGCAGTTCCCCTGGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000155840.12:c.*1058_*1073delinsTGCAGTTCCCCTGGAA (KCNQ1) MANE Select ENSP00000155840.2:n.*1058_*1073delinsTGCAGTTCCCCTGGAA
ENST00000155840.9:c.*1058_*1073delinsTGCAGTTCCCCTGGAA (KCNQ1) ENSP00000155840.2:n.*1058_*1073delinsTGCAGTTCCCCTGGAA
NM_000218.2:c.*1058_*1073delinsTGCAGTTCCCCTGGAA , LRG_287t1:c.*1058_*1073delinsTGCAGTTCCCCTGGAA (KCNQ1) NP_000209.2:n.*1058_*1073delinsTGCAGTTCCCCTGGAA
NM_181798.1:c.*1058_*1073delinsTGCAGTTCCCCTGGAA , LRG_287t2:c.*1058_*1073delinsTGCAGTTCCCCTGGAA (KCNQ1) NP_861463.1:n.*1058_*1073delinsTGCAGTTCCCCTGGAA
NR_130721.1:n.778-8634_778-8619delinsTTCCAGGGGAACTGCA (KCNQ1-AS1)
NM_000218.3:c.*1058_*1073delinsTGCAGTTCCCCTGGAA (KCNQ1) MANE Select NP_000209.2:n.*1058_*1073delinsTGCAGTTCCCCTGGAA