Canonical Allele Identifier: CA216346623
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1050174772
gnomAD v2: 11-2870268-G-T
gnomAD v3: 11-2849038-G-T
gnomAD v4: 11-2849038-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2849038G>T , CM000673.2:g.2849038G>T GRCh38
NC_000011.9:g.2870268G>T , CM000673.1:g.2870268G>T GRCh37
NC_000011.8:g.2826844G>T NCBI36
NG_008935.1:g.409048G>T , LRG_287:g.409048G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000155840.12:c.*1035G>T (KCNQ1) MANE Select ENSP00000155840.2:n.*1035G>T
ENST00000155840.9:c.*1035G>T (KCNQ1) ENSP00000155840.2:n.*1035G>T
NM_000218.2:c.*1035G>T , LRG_287t1:c.*1035G>T (KCNQ1) NP_000209.2:n.*1035G>T
NM_181798.1:c.*1035G>T , LRG_287t2:c.*1035G>T (KCNQ1) NP_861463.1:n.*1035G>T
NR_130721.1:n.778-8596C>A (KCNQ1-AS1)
NM_000218.3:c.*1035G>T (KCNQ1) MANE Select NP_000209.2:n.*1035G>T