Canonical Allele Identifier: CA216334614
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs2237897
gnomAD v2: 11-2858546-C-T
gnomAD v3: 11-2837316-C-T
gnomAD v4: 11-2837316-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2837316C>T , CM000673.2:g.2837316C>T GRCh38
NC_000011.9:g.2858546C>T , CM000673.1:g.2858546C>T GRCh37
NC_000011.8:g.2815122C>T NCBI36
NG_008935.1:g.397326C>T , LRG_287:g.397326C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1438-10451C>T ENSP00000434560.2:n.1438-10451C>T
ENST00000646564.2:c.1255-2400C>T ENSP00000495806.2:n.1255-2400C>T
ENST00000155840.12:c.1795-10451C>T MANE Select ENSP00000155840.2:n.1795-10451C>T
ENST00000335475.6:c.1414-10451C>T ENSP00000334497.5:n.1414-10451C>T
ENST00000526095.2:c.199-10451C>T ENSP00000494939.1:n.199-10451C>T
ENST00000646564.1:c.901-2400C>T ENSP00000495806.1:n.901-2400C>T
ENST00000155840.9:c.1795-10451C>T ENSP00000155840.2:n.1795-10451C>T
ENST00000335475.5:c.1414-10451C>T ENSP00000334497.5:n.1414-10451C>T
ENST00000526095.1:n.302-10451C>T
NM_000218.2:c.1795-10451C>T , LRG_287t1:c.1795-10451C>T NP_000209.2:n.1795-10451C>T
NM_181798.1:c.1414-10451C>T , LRG_287t2:c.1414-10451C>T NP_861463.1:n.1414-10451C>T
NM_000218.3:c.1795-10451C>T MANE Select NP_000209.2:n.1795-10451C>T