Canonical Allele Identifier: CA379135081

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2610028A>T (hg19) ; chr11:g.2588798A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588798A>T , CM000673.2:g.2588798A>T	GRCh38
NC_000011.9:g.2610028A>T , CM000673.1:g.2610028A>T	GRCh37
NC_000011.8:g.2566604A>T	NCBI36
NG_008935.1:g.148808A>T , LRG_287:g.148808A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.980A>T	ENSP00000434560.2:p.Asp327Val
ENST00000646564.2:c.797A>T	ENSP00000495806.2:p.Asp266Val
ENST00000155840.12:c.1337A>T MANE Select	ENSP00000155840.2:p.Asp446Val
ENST00000335475.6:c.956A>T	ENSP00000334497.5:p.Asp319Val
ENST00000646564.1:c.443A>T	ENSP00000495806.1:p.Asp148Val
ENST00000155840.9:c.1337A>T	ENSP00000155840.2:p.Asp446Val
ENST00000335475.5:c.956A>T	ENSP00000334497.5:p.Asp319Val
NM_000218.2:c.1337A>T , LRG_287t1:c.1337A>T	NP_000209.2:p.Asp446Val
NM_181798.1:c.956A>T , LRG_287t2:c.956A>T	NP_861463.1:p.Asp319Val
NM_000218.3:c.1337A>T MANE Select	NP_000209.2:p.Asp446Val