Canonical Allele Identifier: CA1948175000

Gene: KCNQ1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2468112C>A , CM000673.2:g.2468112C>A	GRCh38
NC_000011.9:g.2489342C>A , CM000673.1:g.2489342C>A	GRCh37
NC_000011.8:g.2445918C>A	NCBI36
NG_008935.1:g.28122C>A , LRG_287:g.28122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380776.5:n.91+6135C>A
ENST00000496887.7:c.125+22628C>A	ENSP00000434560.2:n.125+22628C>A
ENST00000646564.2:c.386+22628C>A	ENSP00000495806.2:n.386+22628C>A
ENST00000155840.12:c.386+22628C>A MANE Select	ENSP00000155840.2:n.386+22628C>A
ENST00000335475.6:c.5+6398C>A	ENSP00000334497.5:n.5+6398C>A
ENST00000646564.1:c.32+22628C>A	ENSP00000495806.1:n.32+22628C>A
ENST00000155840.9:c.386+22628C>A	ENSP00000155840.2:n.386+22628C>A
ENST00000335475.5:c.5+6398C>A	ENSP00000334497.5:n.5+6398C>A
ENST00000345015.4:n.163+22628C>A
ENST00000380776.4:c.84+6135C>A	ENSP00000370153.4:n.84+6135C>A
ENST00000496887.6:c.125+22628C>A	ENSP00000434560.1:n.125+22628C>A
NM_000218.2:c.386+22628C>A , LRG_287t1:c.386+22628C>A	NP_000209.2:n.386+22628C>A
NM_181798.1:c.5+6398C>A , LRG_287t2:c.5+6398C>A	NP_861463.1:n.5+6398C>A
NM_000218.3:c.386+22628C>A MANE Select	NP_000209.2:n.386+22628C>A