Canonical Allele Identifier: CA472039102

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2608844C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587614C>A , CM000673.2:g.2587614C>A	GRCh38
NC_000011.9:g.2608844C>A , CM000673.1:g.2608844C>A	GRCh37
NC_000011.8:g.2565420C>A	NCBI36
NG_008935.1:g.147624C>A , LRG_287:g.147624C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.816C>A	ENSP00000434560.2:p.Thr272=
ENST00000646564.2:c.633C>A	ENSP00000495806.2:p.Thr211=
ENST00000155840.12:c.1173C>A MANE Select	ENSP00000155840.2:p.Thr391=
ENST00000335475.6:c.792C>A	ENSP00000334497.5:p.Thr264=
ENST00000646564.1:c.279C>A	ENSP00000495806.1:p.Thr93=
ENST00000155840.9:c.1173C>A	ENSP00000155840.2:p.Thr391=
ENST00000335475.5:c.792C>A	ENSP00000334497.5:p.Thr264=
NM_000218.2:c.1173C>A , LRG_287t1:c.1173C>A	NP_000209.2:p.Thr391=
NM_181798.1:c.792C>A , LRG_287t2:c.792C>A	NP_861463.1:p.Thr264=
NM_000218.3:c.1173C>A MANE Select	NP_000209.2:p.Thr391=