Canonical Allele Identifier: CA379116904
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1846021218
gnomAD v3: 11-2445339-C-T
gnomAD v4: 11-2445339-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445339C>T , CM000673.2:g.2445339C>T GRCh38
NC_000011.9:g.2466569C>T , CM000673.1:g.2466569C>T GRCh37
NC_000011.8:g.2423145C>T NCBI36
NG_008935.1:g.5349C>T , LRG_287:g.5349C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-44C>T ENSP00000434560.2:n.24-44C>T
ENST00000646564.2:c.241C>T ENSP00000495806.2:p.Pro81Ser
ENST00000155840.12:c.241C>T MANE Select ENSP00000155840.2:p.Pro81Ser
ENST00000155840.9:c.241C>T ENSP00000155840.2:p.Pro81Ser
ENST00000345015.4:n.18C>T
ENST00000496887.6:c.24-44C>T ENSP00000434560.1:n.24-44C>T
NM_000218.2:c.241C>T , LRG_287t1:c.241C>T NP_000209.2:p.Pro81Ser
NM_000218.3:c.241C>T MANE Select NP_000209.2:p.Pro81Ser