Canonical Allele Identifier: CA1948273282
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2702479T= , CM000673.2:g.2702479T= GRCh38
NC_000011.9:g.2723709T= , CM000673.1:g.2723709T= GRCh37
NC_000011.8:g.2680285T= NCBI36
NG_008935.1:g.262489T= , LRG_287:g.262489T=
NG_016178.2:g.2520A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1157+40398T= ENSP00000434560.2:n.1157+40398T=
ENST00000646564.2:c.974+40398T= ENSP00000495806.2:n.974+40398T=
ENST00000155840.12:c.1514+40398T= MANE Select ENSP00000155840.2:n.1514+40398T=
ENST00000335475.6:c.1133+40398T= ENSP00000334497.5:n.1133+40398T=
ENST00000646564.1:c.620+40398T= ENSP00000495806.1:n.620+40398T=
ENST00000155840.9:c.1514+40398T= ENSP00000155840.2:n.1514+40398T=
ENST00000335475.5:c.1133+40398T= ENSP00000334497.5:n.1133+40398T=
NM_000218.2:c.1514+40398T= , LRG_287t1:c.1514+40398T= NP_000209.2:n.1514+40398T=
NM_181798.1:c.1133+40398T= , LRG_287t2:c.1133+40398T= NP_861463.1:n.1133+40398T=
NM_000218.3:c.1514+40398T= MANE Select NP_000209.2:n.1514+40398T=