Canonical Allele Identifier: CA472466650
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 11-2847877-G-T
MyVariant Identifiers: chr11:g.2869107G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847877G>T , CM000673.2:g.2847877G>T GRCh38
NC_000011.9:g.2869107G>T , CM000673.1:g.2869107G>T GRCh37
NC_000011.8:g.2825683G>T NCBI36
NG_008935.1:g.407887G>T , LRG_287:g.407887G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1548G>T (KCNQ1) ENSP00000434560.2:p.Gly516=
ENST00000155840.12:c.1905G>T (KCNQ1) MANE Select ENSP00000155840.2:p.Gly635=
ENST00000335475.6:c.1524G>T (KCNQ1) ENSP00000334497.5:p.Gly508=
ENST00000526095.2:c.309G>T (KCNQ1) ENSP00000494939.1:p.Gly103=
ENST00000155840.9:c.1905G>T (KCNQ1) ENSP00000155840.2:p.Gly635=
ENST00000335475.5:c.1524G>T (KCNQ1) ENSP00000334497.5:p.Gly508=
ENST00000526095.1:n.412G>T (KCNQ1)
NM_000218.2:c.1905G>T , LRG_287t1:c.1905G>T (KCNQ1) NP_000209.2:p.Gly635=
NM_181798.1:c.1524G>T , LRG_287t2:c.1524G>T (KCNQ1) NP_861463.1:p.Gly508=
NR_130721.1:n.778-7435C>A (KCNQ1-AS1)
NM_000218.3:c.1905G>T (KCNQ1) MANE Select NP_000209.2:p.Gly635=