Canonical Allele Identifier: CA1948242729
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572081T= , CM000673.2:g.2572081T= GRCh38
NC_000011.9:g.2593311T= , CM000673.1:g.2593311T= GRCh37
NC_000011.8:g.2549887T= NCBI36
NG_008935.1:g.132091T= , LRG_287:g.132091T=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.491T= ENSP00000434560.2:p.Leu164=
ENST00000646564.2:c.478-11354T= ENSP00000495806.2:n.478-11354T=
ENST00000155840.12:c.752T= MANE Select ENSP00000155840.2:p.Leu251=
ENST00000335475.6:c.371T= ENSP00000334497.5:p.Leu124=
ENST00000646564.1:c.124-11354T= ENSP00000495806.1:n.124-11354T=
ENST00000155840.9:c.752T= ENSP00000155840.2:p.Leu251=
ENST00000335475.5:c.371T= ENSP00000334497.5:p.Leu124=
ENST00000496887.6:c.491T= ENSP00000434560.1:p.Leu164=
NM_000218.2:c.752T= , LRG_287t1:c.752T= NP_000209.2:p.Leu251=
NM_181798.1:c.371T= , LRG_287t2:c.371T= NP_861463.1:p.Leu124=
NM_000218.3:c.752T= MANE Select NP_000209.2:p.Leu251=