Canonical Allele Identifier: CA1948236075
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2588803C= , CM000673.2:g.2588803C= GRCh38
NC_000011.9:g.2610033C= , CM000673.1:g.2610033C= GRCh37
NC_000011.8:g.2566609C= NCBI36
NG_008935.1:g.148813C= , LRG_287:g.148813C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.985C= ENSP00000434560.2:p.Pro329=
ENST00000646564.2:c.802C= ENSP00000495806.2:p.Pro268=
ENST00000155840.12:c.1342C= MANE Select ENSP00000155840.2:p.Pro448=
ENST00000335475.6:c.961C= ENSP00000334497.5:p.Pro321=
ENST00000646564.1:c.448C= ENSP00000495806.1:p.Pro150=
ENST00000155840.9:c.1342C= ENSP00000155840.2:p.Pro448=
ENST00000335475.5:c.961C= ENSP00000334497.5:p.Pro321=
NM_000218.2:c.1342C= , LRG_287t1:c.1342C= NP_000209.2:p.Pro448=
NM_181798.1:c.961C= , LRG_287t2:c.961C= NP_861463.1:p.Pro321=
NM_000218.3:c.1342C= MANE Select NP_000209.2:p.Pro448=