Canonical Allele Identifier: CA1948314044
Community Standard Title: NM_000218.3(KCNQ1):c.1637C= (p.Ser546=)
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2776006C= , CM000673.2:g.2776006C= GRCh38
NC_000011.9:g.2797236C= , CM000673.1:g.2797236C= GRCh37
NC_000011.8:g.2753812C= NCBI36
NG_008935.1:g.336016C= , LRG_287:g.336016C=

Transcript Alleles

HGVS Amino-acid Change
NM_000218.3:c.1637C= MANE Select NP_000209.2:p.Ser546=
ENST00000155840.12:c.1637C= MANE Select ENSP00000155840.2:p.Ser546=
NM_000218.2:c.1637C= , LRG_287t1:c.1637C= NP_000209.2:p.Ser546=
NM_181798.1:c.1256C= , LRG_287t2:c.1256C= NP_861463.1:p.Ser419=
ENST00000155840.9:c.1637C= ENSP00000155840.2:p.Ser546=
ENST00000335475.5:c.1256C= ENSP00000334497.5:p.Ser419=
ENST00000335475.6:c.1256C= ENSP00000334497.5:p.Ser419=
ENST00000496887.7:c.1280C= ENSP00000434560.2:p.Ser427=
ENST00000646564.1:c.743C= ENSP00000495806.1:p.Ser248=
ENST00000646564.2:c.1097C= ENSP00000495806.2:p.Ser366=