Canonical Allele Identifier: CA2723272787
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2134096573
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847681T>C , CM000673.2:g.2847681T>C GRCh38
NC_000011.9:g.2868911T>C , CM000673.1:g.2868911T>C GRCh37
NC_000011.8:g.2825487T>C NCBI36
NG_008935.1:g.407691T>C , LRG_287:g.407691T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1438-86T>C (KCNQ1) ENSP00000434560.2:n.1438-86T>C
ENST00000155840.12:c.1795-86T>C (KCNQ1) MANE Select ENSP00000155840.2:n.1795-86T>C
ENST00000335475.6:c.1414-86T>C (KCNQ1) ENSP00000334497.5:n.1414-86T>C
ENST00000526095.2:c.199-86T>C (KCNQ1) ENSP00000494939.1:n.199-86T>C
ENST00000155840.9:c.1795-86T>C (KCNQ1) ENSP00000155840.2:n.1795-86T>C
ENST00000335475.5:c.1414-86T>C (KCNQ1) ENSP00000334497.5:n.1414-86T>C
ENST00000526095.1:n.302-86T>C (KCNQ1)
NM_000218.2:c.1795-86T>C , LRG_287t1:c.1795-86T>C (KCNQ1) NP_000209.2:n.1795-86T>C
NM_181798.1:c.1414-86T>C , LRG_287t2:c.1414-86T>C (KCNQ1) NP_861463.1:n.1414-86T>C
NR_130721.1:n.778-7239A>G (KCNQ1-AS1)
NM_000218.3:c.1795-86T>C (KCNQ1) MANE Select NP_000209.2:n.1795-86T>C
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