Canonical Allele Identifier: CA379140376
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 879033
dbSNP Id: rs1848365419
gnomAD v4: 11-2847867-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847867G>A , CM000673.2:g.2847867G>A GRCh38
NC_000011.9:g.2869097G>A , CM000673.1:g.2869097G>A GRCh37
NC_000011.8:g.2825673G>A NCBI36
NG_008935.1:g.407877G>A , LRG_287:g.407877G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1538G>A (KCNQ1) ENSP00000434560.2:p.Arg513Lys
ENST00000155840.12:c.1895G>A (KCNQ1) MANE Select ENSP00000155840.2:p.Arg632Lys
ENST00000335475.6:c.1514G>A (KCNQ1) ENSP00000334497.5:p.Arg505Lys
ENST00000526095.2:c.299G>A (KCNQ1) ENSP00000494939.1:p.Arg100Lys
ENST00000155840.9:c.1895G>A (KCNQ1) ENSP00000155840.2:p.Arg632Lys
ENST00000335475.5:c.1514G>A (KCNQ1) ENSP00000334497.5:p.Arg505Lys
ENST00000526095.1:n.402G>A (KCNQ1)
NM_000218.2:c.1895G>A , LRG_287t1:c.1895G>A (KCNQ1) NP_000209.2:p.Arg632Lys
NM_181798.1:c.1514G>A , LRG_287t2:c.1514G>A (KCNQ1) NP_861463.1:p.Arg505Lys
NR_130721.1:n.778-7425C>T (KCNQ1-AS1)
NM_000218.3:c.1895G>A (KCNQ1) MANE Select NP_000209.2:p.Arg632Lys