Canonical Allele Identifier: CA1948349527
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1564916301
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847682C>G , CM000673.2:g.2847682C>G GRCh38
NC_000011.9:g.2868912C>G , CM000673.1:g.2868912C>G GRCh37
NC_000011.8:g.2825488C>G NCBI36
NG_008935.1:g.407692C>G , LRG_287:g.407692C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1438-85C>G (KCNQ1) ENSP00000434560.2:n.1438-85C>G
ENST00000155840.12:c.1795-85C>G (KCNQ1) MANE Select ENSP00000155840.2:n.1795-85C>G
ENST00000335475.6:c.1414-85C>G (KCNQ1) ENSP00000334497.5:n.1414-85C>G
ENST00000526095.2:c.199-85C>G (KCNQ1) ENSP00000494939.1:n.199-85C>G
ENST00000155840.9:c.1795-85C>G (KCNQ1) ENSP00000155840.2:n.1795-85C>G
ENST00000335475.5:c.1414-85C>G (KCNQ1) ENSP00000334497.5:n.1414-85C>G
ENST00000526095.1:n.302-85C>G (KCNQ1)
NM_000218.2:c.1795-85C>G , LRG_287t1:c.1795-85C>G (KCNQ1) NP_000209.2:n.1795-85C>G
NM_181798.1:c.1414-85C>G , LRG_287t2:c.1414-85C>G (KCNQ1) NP_861463.1:n.1414-85C>G
NR_130721.1:n.778-7240G>C (KCNQ1-AS1)
NM_000218.3:c.1795-85C>G (KCNQ1) MANE Select NP_000209.2:n.1795-85C>G
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