Canonical Allele Identifier: CA1948309479

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1846533906

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768408G>A , CM000673.2:g.2768408G>A	GRCh38
NC_000011.9:g.2789638G>A , CM000673.1:g.2789638G>A	GRCh37
NC_000011.8:g.2746214G>A	NCBI36
NG_008935.1:g.328418G>A , LRG_287:g.328418G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1158-436G>A	ENSP00000434560.2:n.1158-436G>A
ENST00000646564.2:c.975-436G>A	ENSP00000495806.2:n.975-436G>A
ENST00000155840.12:c.1515-436G>A MANE Select	ENSP00000155840.2:n.1515-436G>A
ENST00000335475.6:c.1134-436G>A	ENSP00000334497.5:n.1134-436G>A
ENST00000646564.1:c.621-436G>A	ENSP00000495806.1:n.621-436G>A
ENST00000155840.9:c.1515-436G>A	ENSP00000155840.2:n.1515-436G>A
ENST00000335475.5:c.1134-436G>A	ENSP00000334497.5:n.1134-436G>A
NM_000218.2:c.1515-436G>A , LRG_287t1:c.1515-436G>A	NP_000209.2:n.1515-436G>A
NM_181798.1:c.1134-436G>A , LRG_287t2:c.1134-436G>A	NP_861463.1:n.1134-436G>A
NM_000218.3:c.1515-436G>A MANE Select	NP_000209.2:n.1515-436G>A