Canonical Allele Identifier: CA2612011721
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848165_2848166insGTC , CM000673.2:g.2848165_2848166insGTC GRCh38
NC_000011.9:g.2869395_2869396insGTC , CM000673.1:g.2869395_2869396insGTC GRCh37
NC_000011.8:g.2825971_2825972insGTC NCBI36
NG_008935.1:g.408175_408176insGTC , LRG_287:g.408175_408176insGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.*162_*163insGTC (KCNQ1) ENSP00000434560.2:n.*162_*163insGTC
ENST00000155840.12:c.*162_*163insGTC (KCNQ1) MANE Select ENSP00000155840.2:n.*162_*163insGTC
ENST00000335475.6:c.*162_*163insGTC (KCNQ1) ENSP00000334497.5:n.*162_*163insGTC
ENST00000526095.2:c.*162_*163insGTC (KCNQ1) ENSP00000494939.1:n.*162_*163insGTC
ENST00000155840.9:c.*162_*163insGTC (KCNQ1) ENSP00000155840.2:n.*162_*163insGTC
ENST00000335475.5:c.*162_*163insGTC (KCNQ1) ENSP00000334497.5:n.*162_*163insGTC
ENST00000526095.1:n.700_701insGTC (KCNQ1)
NM_000218.2:c.*162_*163insGTC , LRG_287t1:c.*162_*163insGTC (KCNQ1) NP_000209.2:n.*162_*163insGTC
NM_181798.1:c.*162_*163insGTC , LRG_287t2:c.*162_*163insGTC (KCNQ1) NP_861463.1:n.*162_*163insGTC
NR_130721.1:n.778-7724_778-7723insGAC (KCNQ1-AS1)
NM_000218.3:c.*162_*163insGTC (KCNQ1) MANE Select NP_000209.2:n.*162_*163insGTC