Canonical Allele Identifier: CA379133001
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583471C>A , CM000673.2:g.2583471C>A GRCh38
NC_000011.9:g.2604701C>A , CM000673.1:g.2604701C>A GRCh37
NC_000011.8:g.2561277C>A NCBI36
NG_008935.1:g.143481C>A , LRG_287:g.143481C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.697C>A ENSP00000434560.2:p.Pro233Thr
ENST00000646564.2:c.514C>A ENSP00000495806.2:p.Pro172Thr
ENST00000155840.12:c.958C>A MANE Select ENSP00000155840.2:p.Pro320Thr
ENST00000335475.6:c.577C>A ENSP00000334497.5:p.Pro193Thr
ENST00000646564.1:c.160C>A ENSP00000495806.1:p.Pro54Thr
ENST00000155840.9:c.958C>A ENSP00000155840.2:p.Pro320Thr
ENST00000335475.5:c.577C>A ENSP00000334497.5:p.Pro193Thr
NM_000218.2:c.958C>A , LRG_287t1:c.958C>A NP_000209.2:p.Pro320Thr
NM_181798.1:c.577C>A , LRG_287t2:c.577C>A NP_861463.1:p.Pro193Thr
NM_000218.3:c.958C>A MANE Select NP_000209.2:p.Pro320Thr