Canonical Allele Identifier: CA653931184
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

COSMIC: COSN15676195
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848609_2848610insC , CM000673.2:g.2848609_2848610insC GRCh38
NC_000011.9:g.2869839_2869840insC , CM000673.1:g.2869839_2869840insC GRCh37
NC_000011.8:g.2826415_2826416insC NCBI36
NG_008935.1:g.408619_408620insC , LRG_287:g.408619_408620insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.*606_*607insC (KCNQ1) ENSP00000434560.2:n.*606_*607insC
ENST00000155840.12:c.*606_*607insC (KCNQ1) MANE Select ENSP00000155840.2:n.*606_*607insC
ENST00000335475.6:c.*606_*607insC (KCNQ1) ENSP00000334497.5:n.*606_*607insC
ENST00000155840.9:c.*606_*607insC (KCNQ1) ENSP00000155840.2:n.*606_*607insC
NM_000218.2:c.*606_*607insC , LRG_287t1:c.*606_*607insC (KCNQ1) NP_000209.2:n.*606_*607insC
NM_181798.1:c.*606_*607insC , LRG_287t2:c.*606_*607insC (KCNQ1) NP_861463.1:n.*606_*607insC
NR_130721.1:n.778-8168_778-8167insG (KCNQ1-AS1)
NM_000218.3:c.*606_*607insC (KCNQ1) MANE Select NP_000209.2:n.*606_*607insC
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