Canonical Allele Identifier: CA1948350250
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs10798
gnomAD v4: 11-2848935-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848935A>C , CM000673.2:g.2848935A>C GRCh38
NC_000011.9:g.2870165A>C , CM000673.1:g.2870165A>C GRCh37
NC_000011.8:g.2826741A>C NCBI36
NG_008935.1:g.408945A>C , LRG_287:g.408945A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.*932A>C (KCNQ1) ENSP00000434560.2:n.*932A>C
ENST00000155840.12:c.*932A>C (KCNQ1) MANE Select ENSP00000155840.2:n.*932A>C
ENST00000335475.6:c.*932A>C (KCNQ1) ENSP00000334497.5:n.*932A>C
ENST00000155840.9:c.*932A>C (KCNQ1) ENSP00000155840.2:n.*932A>C
NM_000218.2:c.*932A>C , LRG_287t1:c.*932A>C (KCNQ1) NP_000209.2:n.*932A>C
NM_181798.1:c.*932A>C , LRG_287t2:c.*932A>C (KCNQ1) NP_861463.1:n.*932A>C
NR_130721.1:n.778-8493T>G (KCNQ1-AS1)
NM_000218.3:c.*932A>C (KCNQ1) MANE Select NP_000209.2:n.*932A>C