Canonical Allele Identifier: CA1948292233

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1845856448

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2731391C>A , CM000673.2:g.2731391C>A	GRCh38
NC_000011.9:g.2752621C>A , CM000673.1:g.2752621C>A	GRCh37
NC_000011.8:g.2709197C>A	NCBI36
NG_008935.1:g.291401C>A , LRG_287:g.291401C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1158-37453C>A	ENSP00000434560.2:n.1158-37453C>A
ENST00000646564.2:c.975-37453C>A	ENSP00000495806.2:n.975-37453C>A
ENST00000155840.12:c.1515-37453C>A MANE Select	ENSP00000155840.2:n.1515-37453C>A
ENST00000335475.6:c.1134-37453C>A	ENSP00000334497.5:n.1134-37453C>A
ENST00000646564.1:c.621-37453C>A	ENSP00000495806.1:n.621-37453C>A
ENST00000155840.9:c.1515-37453C>A	ENSP00000155840.2:n.1515-37453C>A
ENST00000335475.5:c.1134-37453C>A	ENSP00000334497.5:n.1134-37453C>A
NM_000218.2:c.1515-37453C>A , LRG_287t1:c.1515-37453C>A	NP_000209.2:n.1515-37453C>A
NM_181798.1:c.1134-37453C>A , LRG_287t2:c.1134-37453C>A	NP_861463.1:n.1134-37453C>A
NM_000218.3:c.1515-37453C>A MANE Select	NP_000209.2:n.1515-37453C>A