Canonical Allele Identifier: CA1948243199
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572896G= , CM000673.2:g.2572896G= GRCh38
NC_000011.9:g.2594126G= , CM000673.1:g.2594126G= GRCh37
NC_000011.8:g.2550702G= NCBI36
NG_008935.1:g.132906G= , LRG_287:g.132906G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.570G= ENSP00000434560.2:p.Ser190=
ENST00000646564.2:c.478-10539G= ENSP00000495806.2:n.478-10539G=
ENST00000155840.12:c.831G= MANE Select ENSP00000155840.2:p.Ser277=
ENST00000335475.6:c.450G= ENSP00000334497.5:p.Ser150=
ENST00000646564.1:c.124-10539G= ENSP00000495806.1:n.124-10539G=
ENST00000155840.9:c.831G= ENSP00000155840.2:p.Ser277=
ENST00000335475.5:c.450G= ENSP00000334497.5:p.Ser150=
ENST00000496887.6:c.570G= ENSP00000434560.1:p.Ser190=
NM_000218.2:c.831G= , LRG_287t1:c.831G= NP_000209.2:p.Ser277=
NM_181798.1:c.450G= , LRG_287t2:c.450G= NP_861463.1:p.Ser150=
NM_000218.3:c.831G= MANE Select NP_000209.2:p.Ser277=