Canonical Allele Identifier: CA2841921258

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587556C>A , CM000673.2:g.2587556C>A	GRCh38
NC_000011.9:g.2608786C>A , CM000673.1:g.2608786C>A	GRCh37
NC_000011.8:g.2565362C>A	NCBI36
NG_008935.1:g.147566C>A , LRG_287:g.147566C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.772-14C>A	ENSP00000434560.2:n.772-14C>A
ENST00000646564.2:c.589-14C>A	ENSP00000495806.2:n.589-14C>A
ENST00000155840.12:c.1129-14C>A MANE Select	ENSP00000155840.2:n.1129-14C>A
ENST00000335475.6:c.748-14C>A	ENSP00000334497.5:n.748-14C>A
ENST00000646564.1:c.235-14C>A	ENSP00000495806.1:n.235-14C>A
ENST00000155840.9:c.1129-14C>A	ENSP00000155840.2:n.1129-14C>A
ENST00000335475.5:c.748-14C>A	ENSP00000334497.5:n.748-14C>A
NM_000218.2:c.1129-14C>A , LRG_287t1:c.1129-14C>A	NP_000209.2:n.1129-14C>A
NM_181798.1:c.748-14C>A , LRG_287t2:c.748-14C>A	NP_861463.1:n.748-14C>A
NM_000218.3:c.1129-14C>A MANE Select	NP_000209.2:n.1129-14C>A