Canonical Allele Identifier: CA1948225165
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583541C= , CM000673.2:g.2583541C= GRCh38
NC_000011.9:g.2604771C= , CM000673.1:g.2604771C= GRCh37
NC_000011.8:g.2561347C= NCBI36
NG_008935.1:g.143551C= , LRG_287:g.143551C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.767C= ENSP00000434560.2:p.Pro256=
ENST00000646564.2:c.584C= ENSP00000495806.2:p.Pro195=
ENST00000155840.12:c.1028C= MANE Select ENSP00000155840.2:p.Pro343=
ENST00000335475.6:c.647C= ENSP00000334497.5:p.Pro216=
ENST00000646564.1:c.230C= ENSP00000495806.1:p.Pro77=
ENST00000155840.9:c.1028C= ENSP00000155840.2:p.Pro343=
ENST00000335475.5:c.647C= ENSP00000334497.5:p.Pro216=
NM_000218.2:c.1028C= , LRG_287t1:c.1028C= NP_000209.2:p.Pro343=
NM_181798.1:c.647C= , LRG_287t2:c.647C= NP_861463.1:p.Pro216=
NM_000218.3:c.1028C= MANE Select NP_000209.2:p.Pro343=