Canonical Allele Identifier: CA1948349655
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847876G= , CM000673.2:g.2847876G= GRCh38
NC_000011.9:g.2869106G= , CM000673.1:g.2869106G= GRCh37
NC_000011.8:g.2825682G= NCBI36
NG_008935.1:g.407886G= , LRG_287:g.407886G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1547G= (KCNQ1) ENSP00000434560.2:p.Gly516=
ENST00000155840.12:c.1904G= (KCNQ1) MANE Select ENSP00000155840.2:p.Gly635=
ENST00000335475.6:c.1523G= (KCNQ1) ENSP00000334497.5:p.Gly508=
ENST00000526095.2:c.308G= (KCNQ1) ENSP00000494939.1:p.Gly103=
ENST00000155840.9:c.1904G= (KCNQ1) ENSP00000155840.2:p.Gly635=
ENST00000335475.5:c.1523G= (KCNQ1) ENSP00000334497.5:p.Gly508=
ENST00000526095.1:n.411G= (KCNQ1)
NM_000218.2:c.1904G= , LRG_287t1:c.1904G= (KCNQ1) NP_000209.2:p.Gly635=
NM_181798.1:c.1523G= , LRG_287t2:c.1523G= (KCNQ1) NP_861463.1:p.Gly508=
NR_130721.1:n.778-7434C= (KCNQ1-AS1)
NM_000218.3:c.1904G= (KCNQ1) MANE Select NP_000209.2:p.Gly635=