Canonical Allele Identifier: CA379140213
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 11-2847786-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847786G>T , CM000673.2:g.2847786G>T GRCh38
NC_000011.9:g.2869016G>T , CM000673.1:g.2869016G>T GRCh37
NC_000011.8:g.2825592G>T NCBI36
NG_008935.1:g.407796G>T , LRG_287:g.407796G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1457G>T (KCNQ1) ENSP00000434560.2:p.Arg486Met
ENST00000155840.12:c.1814G>T (KCNQ1) MANE Select ENSP00000155840.2:p.Arg605Met
ENST00000335475.6:c.1433G>T (KCNQ1) ENSP00000334497.5:p.Arg478Met
ENST00000526095.2:c.218G>T (KCNQ1) ENSP00000494939.1:p.Arg73Met
ENST00000155840.9:c.1814G>T (KCNQ1) ENSP00000155840.2:p.Arg605Met
ENST00000335475.5:c.1433G>T (KCNQ1) ENSP00000334497.5:p.Arg478Met
ENST00000526095.1:n.321G>T (KCNQ1)
NM_000218.2:c.1814G>T , LRG_287t1:c.1814G>T (KCNQ1) NP_000209.2:p.Arg605Met
NM_181798.1:c.1433G>T , LRG_287t2:c.1433G>T (KCNQ1) NP_861463.1:p.Arg478Met
NR_130721.1:n.778-7344C>A (KCNQ1-AS1)
NM_000218.3:c.1814G>T (KCNQ1) MANE Select NP_000209.2:p.Arg605Met