Canonical Allele Identifier: CA216345281

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• dbSNP Id: rs1034750120
• gnomAD v2: 11-2869119-C-A
• gnomAD v3: 11-2847889-C-A
• gnomAD v4: 11-2847889-C-A
• MyVariant Identifiers: chr11:g.2869119C>A (hg19) ; chr11:g.2847889C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2847889C>A , CM000673.2:g.2847889C>A	GRCh38
NC_000011.9:g.2869119C>A , CM000673.1:g.2869119C>A	GRCh37
NC_000011.8:g.2825695C>A	NCBI36
NG_008935.1:g.407899C>A , LRG_287:g.407899C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1560C>A (KCNQ1)	ENSP00000434560.2:p.Thr520=
ENST00000155840.12:c.1917C>A (KCNQ1) MANE Select	ENSP00000155840.2:p.Thr639=
ENST00000335475.6:c.1536C>A (KCNQ1)	ENSP00000334497.5:p.Thr512=
ENST00000526095.2:c.321C>A (KCNQ1)	ENSP00000494939.1:p.Thr107=
ENST00000155840.9:c.1917C>A (KCNQ1)	ENSP00000155840.2:p.Thr639=
ENST00000335475.5:c.1536C>A (KCNQ1)	ENSP00000334497.5:p.Thr512=
ENST00000526095.1:n.424C>A (KCNQ1)
NM_000218.2:c.1917C>A , LRG_287t1:c.1917C>A (KCNQ1)	NP_000209.2:p.Thr639=
NM_181798.1:c.1536C>A , LRG_287t2:c.1536C>A (KCNQ1)	NP_861463.1:p.Thr512=
NR_130721.1:n.778-7447G>T (KCNQ1-AS1)
NM_000218.3:c.1917C>A (KCNQ1) MANE Select	NP_000209.2:p.Thr639=