Canonical Allele Identifier: CA1948242558

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1848342206

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572002C>G , CM000673.2:g.2572002C>G	GRCh38
NC_000011.9:g.2593232C>G , CM000673.1:g.2593232C>G	GRCh37
NC_000011.8:g.2549808C>G	NCBI36
NG_008935.1:g.132012C>G , LRG_287:g.132012C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.423-11C>G	ENSP00000434560.2:n.423-11C>G
ENST00000646564.2:c.478-11433C>G	ENSP00000495806.2:n.478-11433C>G
ENST00000155840.12:c.684-11C>G MANE Select	ENSP00000155840.2:n.684-11C>G
ENST00000335475.6:c.303-11C>G	ENSP00000334497.5:n.303-11C>G
ENST00000646564.1:c.124-11433C>G	ENSP00000495806.1:n.124-11433C>G
ENST00000155840.9:c.684-11C>G	ENSP00000155840.2:n.684-11C>G
ENST00000335475.5:c.303-11C>G	ENSP00000334497.5:n.303-11C>G
ENST00000496887.6:c.423-11C>G	ENSP00000434560.1:n.423-11C>G
NM_000218.2:c.684-11C>G , LRG_287t1:c.684-11C>G	NP_000209.2:n.684-11C>G
NM_181798.1:c.303-11C>G , LRG_287t2:c.303-11C>G	NP_861463.1:n.303-11C>G
NM_000218.3:c.684-11C>G MANE Select	NP_000209.2:n.684-11C>G