Canonical Allele Identifier: CA379122020

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549228A>G (hg19) ; chr11:g.2527998A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527998A>G , CM000673.2:g.2527998A>G	GRCh38
NC_000011.9:g.2549228A>G , CM000673.1:g.2549228A>G	GRCh37
NC_000011.8:g.2505804A>G	NCBI36
NG_008935.1:g.88008A>G , LRG_287:g.88008A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.196A>G	ENSP00000434560.2:p.Thr66Ala
ENST00000646564.2:c.457A>G	ENSP00000495806.2:p.Thr153Ala
ENST00000155840.12:c.457A>G MANE Select	ENSP00000155840.2:p.Thr153Ala
ENST00000335475.6:c.76A>G	ENSP00000334497.5:p.Thr26Ala
ENST00000646564.1:c.103A>G	ENSP00000495806.1:p.Thr35Ala
ENST00000155840.9:c.457A>G	ENSP00000155840.2:p.Thr153Ala
ENST00000335475.5:c.76A>G	ENSP00000334497.5:p.Thr26Ala
ENST00000496887.6:c.196A>G	ENSP00000434560.1:p.Thr66Ala
NM_000218.2:c.457A>G , LRG_287t1:c.457A>G	NP_000209.2:p.Thr153Ala
NM_181798.1:c.76A>G , LRG_287t2:c.76A>G	NP_861463.1:p.Thr26Ala
NM_000218.3:c.457A>G MANE Select	NP_000209.2:p.Thr153Ala