Canonical Allele Identifier: CA472768118
Gene: KCNQ1 HGNC NCBI
KCNQ1OT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2691378A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2670148A>G , CM000673.2:g.2670148A>G GRCh38
NC_000011.9:g.2691378A>G , CM000673.1:g.2691378A>G GRCh37
NC_000011.8:g.2647954A>G NCBI36
NG_008935.1:g.230158A>G , LRG_287:g.230158A>G
NG_016178.2:g.34851T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1157+8067A>G (KCNQ1) ENSP00000434560.2:n.1157+8067A>G
ENST00000646564.2:c.974+8067A>G (KCNQ1) ENSP00000495806.2:n.974+8067A>G
ENST00000155840.12:c.1514+8067A>G (KCNQ1) MANE Select ENSP00000155840.2:n.1514+8067A>G
ENST00000335475.6:c.1133+8067A>G (KCNQ1) ENSP00000334497.5:n.1133+8067A>G
ENST00000646564.1:c.620+8067A>G (KCNQ1) ENSP00000495806.1:n.620+8067A>G
ENST00000155840.9:c.1514+8067A>G (KCNQ1) ENSP00000155840.2:n.1514+8067A>G
ENST00000335475.5:c.1133+8067A>G (KCNQ1) ENSP00000334497.5:n.1133+8067A>G
NM_000218.2:c.1514+8067A>G , LRG_287t1:c.1514+8067A>G (KCNQ1) NP_000209.2:n.1514+8067A>G
NM_181798.1:c.1133+8067A>G , LRG_287t2:c.1133+8067A>G (KCNQ1) NP_861463.1:n.1133+8067A>G
NR_002728.3:n.29851T>C (KCNQ1OT1)
NM_000218.3:c.1514+8067A>G (KCNQ1) MANE Select NP_000209.2:n.1514+8067A>G