Canonical Allele Identifier: CA1948243139
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572804C= , CM000673.2:g.2572804C= GRCh38
NC_000011.9:g.2594034C= , CM000673.1:g.2594034C= GRCh37
NC_000011.8:g.2550610C= NCBI36
NG_008935.1:g.132814C= , LRG_287:g.132814C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.520-42C= ENSP00000434560.2:n.520-42C=
ENST00000646564.2:c.478-10631C= ENSP00000495806.2:n.478-10631C=
ENST00000155840.12:c.781-42C= MANE Select ENSP00000155840.2:n.781-42C=
ENST00000335475.6:c.400-42C= ENSP00000334497.5:n.400-42C=
ENST00000646564.1:c.124-10631C= ENSP00000495806.1:n.124-10631C=
ENST00000155840.9:c.781-42C= ENSP00000155840.2:n.781-42C=
ENST00000335475.5:c.400-42C= ENSP00000334497.5:n.400-42C=
ENST00000496887.6:c.520-42C= ENSP00000434560.1:n.520-42C=
NM_000218.2:c.781-42C= , LRG_287t1:c.781-42C= NP_000209.2:n.781-42C=
NM_181798.1:c.400-42C= , LRG_287t2:c.400-42C= NP_861463.1:n.400-42C=
NM_000218.3:c.781-42C= MANE Select NP_000209.2:n.781-42C=