Canonical Allele Identifier: CA1948336772
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2822961T= , CM000673.2:g.2822961T= GRCh38
NC_000011.9:g.2844191T= , CM000673.1:g.2844191T= GRCh37
NC_000011.8:g.2800767T= NCBI36
NG_008935.1:g.382971T= , LRG_287:g.382971T=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1438-24806T= ENSP00000434560.2:n.1438-24806T=
ENST00000646564.2:c.1255-16755T= ENSP00000495806.2:n.1255-16755T=
ENST00000155840.12:c.1795-24806T= MANE Select ENSP00000155840.2:n.1795-24806T=
ENST00000335475.6:c.1414-24806T= ENSP00000334497.5:n.1414-24806T=
ENST00000526095.2:c.199-24806T= ENSP00000494939.1:n.199-24806T=
ENST00000646564.1:c.901-16755T= ENSP00000495806.1:n.901-16755T=
ENST00000155840.9:c.1795-24806T= ENSP00000155840.2:n.1795-24806T=
ENST00000335475.5:c.1414-24806T= ENSP00000334497.5:n.1414-24806T=
ENST00000526095.1:n.302-24806T=
NM_000218.2:c.1795-24806T= , LRG_287t1:c.1795-24806T= NP_000209.2:n.1795-24806T=
NM_181798.1:c.1414-24806T= , LRG_287t2:c.1414-24806T= NP_861463.1:n.1414-24806T=
NM_000218.3:c.1795-24806T= MANE Select NP_000209.2:n.1795-24806T=