Canonical Allele Identifier: CA379134650
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587577G>A , CM000673.2:g.2587577G>A GRCh38
NC_000011.9:g.2608807G>A , CM000673.1:g.2608807G>A GRCh37
NC_000011.8:g.2565383G>A NCBI36
NG_008935.1:g.147587G>A , LRG_287:g.147587G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.779G>A ENSP00000434560.2:p.Trp260Ter
ENST00000646564.2:c.596G>A ENSP00000495806.2:p.Trp199Ter
ENST00000155840.12:c.1136G>A MANE Select ENSP00000155840.2:p.Trp379Ter
ENST00000335475.6:c.755G>A ENSP00000334497.5:p.Trp252Ter
ENST00000646564.1:c.242G>A ENSP00000495806.1:p.Trp81Ter
ENST00000155840.9:c.1136G>A ENSP00000155840.2:p.Trp379Ter
ENST00000335475.5:c.755G>A ENSP00000334497.5:p.Trp252Ter
NM_000218.2:c.1136G>A , LRG_287t1:c.1136G>A NP_000209.2:p.Trp379Ter
NM_181798.1:c.755G>A , LRG_287t2:c.755G>A NP_861463.1:p.Trp252Ter
NM_000218.3:c.1136G>A MANE Select NP_000209.2:p.Trp379Ter