Canonical Allele Identifier: CA1948224833
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583469T= , CM000673.2:g.2583469T= GRCh38
NC_000011.9:g.2604699T= , CM000673.1:g.2604699T= GRCh37
NC_000011.8:g.2561275T= NCBI36
NG_008935.1:g.143479T= , LRG_287:g.143479T=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.695T= ENSP00000434560.2:p.Val232=
ENST00000646564.2:c.512T= ENSP00000495806.2:p.Val171=
ENST00000155840.12:c.956T= MANE Select ENSP00000155840.2:p.Val319=
ENST00000335475.6:c.575T= ENSP00000334497.5:p.Val192=
ENST00000646564.1:c.158T= ENSP00000495806.1:p.Val53=
ENST00000155840.9:c.956T= ENSP00000155840.2:p.Val319=
ENST00000335475.5:c.575T= ENSP00000334497.5:p.Val192=
NM_000218.2:c.956T= , LRG_287t1:c.956T= NP_000209.2:p.Val319=
NM_181798.1:c.575T= , LRG_287t2:c.575T= NP_861463.1:p.Val192=
NM_000218.3:c.956T= MANE Select NP_000209.2:p.Val319=