Canonical Allele Identifier: CA379130997

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593298A>C (hg19) ; chr11:g.2572068A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572068A>C , CM000673.2:g.2572068A>C	GRCh38
NC_000011.9:g.2593298A>C , CM000673.1:g.2593298A>C	GRCh37
NC_000011.8:g.2549874A>C	NCBI36
NG_008935.1:g.132078A>C , LRG_287:g.132078A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.478A>C	ENSP00000434560.2:p.Thr160Pro
ENST00000646564.2:c.478-11367A>C	ENSP00000495806.2:n.478-11367A>C
ENST00000155840.12:c.739A>C MANE Select	ENSP00000155840.2:p.Thr247Pro
ENST00000335475.6:c.358A>C	ENSP00000334497.5:p.Thr120Pro
ENST00000646564.1:c.124-11367A>C	ENSP00000495806.1:n.124-11367A>C
ENST00000155840.9:c.739A>C	ENSP00000155840.2:p.Thr247Pro
ENST00000335475.5:c.358A>C	ENSP00000334497.5:p.Thr120Pro
ENST00000496887.6:c.478A>C	ENSP00000434560.1:p.Thr160Pro
NM_000218.2:c.739A>C , LRG_287t1:c.739A>C	NP_000209.2:p.Thr247Pro
NM_181798.1:c.358A>C , LRG_287t2:c.358A>C	NP_861463.1:p.Thr120Pro
NM_000218.3:c.739A>C MANE Select	NP_000209.2:p.Thr247Pro