Canonical Allele Identifier: CA1948309753
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2768803A= , CM000673.2:g.2768803A= GRCh38
NC_000011.9:g.2790033A= , CM000673.1:g.2790033A= GRCh37
NC_000011.8:g.2746609A= NCBI36
NG_008935.1:g.328813A= , LRG_287:g.328813A=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1158-41A= ENSP00000434560.2:n.1158-41A=
ENST00000646564.2:c.975-41A= ENSP00000495806.2:n.975-41A=
ENST00000155840.12:c.1515-41A= MANE Select ENSP00000155840.2:n.1515-41A=
ENST00000335475.6:c.1134-41A= ENSP00000334497.5:n.1134-41A=
ENST00000646564.1:c.621-41A= ENSP00000495806.1:n.621-41A=
ENST00000155840.9:c.1515-41A= ENSP00000155840.2:n.1515-41A=
ENST00000335475.5:c.1134-41A= ENSP00000334497.5:n.1134-41A=
NM_000218.2:c.1515-41A= , LRG_287t1:c.1515-41A= NP_000209.2:n.1515-41A=
NM_181798.1:c.1134-41A= , LRG_287t2:c.1134-41A= NP_861463.1:n.1134-41A=
NM_000218.3:c.1515-41A= MANE Select NP_000209.2:n.1515-41A=