Canonical Allele Identifier: CA379133003
Community Standard Title: NM_000218.3(KCNQ1):c.959C>T (p.Pro320Leu)
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583472C>T , CM000673.2:g.2583472C>T GRCh38
NC_000011.9:g.2604702C>T , CM000673.1:g.2604702C>T GRCh37
NC_000011.8:g.2561278C>T NCBI36
NG_008935.1:g.143482C>T , LRG_287:g.143482C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000218.3:c.959C>T MANE Select NP_000209.2:p.Pro320Leu
ENST00000155840.12:c.959C>T MANE Select ENSP00000155840.2:p.Pro320Leu
NM_000218.2:c.959C>T , LRG_287t1:c.959C>T NP_000209.2:p.Pro320Leu
NM_181798.1:c.578C>T , LRG_287t2:c.578C>T NP_861463.1:p.Pro193Leu
ENST00000155840.9:c.959C>T ENSP00000155840.2:p.Pro320Leu
ENST00000335475.5:c.578C>T ENSP00000334497.5:p.Pro193Leu
ENST00000335475.6:c.578C>T ENSP00000334497.5:p.Pro193Leu
ENST00000496887.7:c.698C>T ENSP00000434560.2:p.Pro233Leu
ENST00000646564.1:c.161C>T ENSP00000495806.1:p.Pro54Leu
ENST00000646564.2:c.515C>T ENSP00000495806.2:p.Pro172Leu