Canonical Allele Identifier: CA379479552

Gene: KCNQ1 KCNQ1OT1

Linked Data

• MyVariant Identifiers: chr11:g.2683240A>C (hg19) ; chr11:g.2662010A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662010A>C , CM000673.2:g.2662010A>C	GRCh38
NC_000011.9:g.2683240A>C , CM000673.1:g.2683240A>C	GRCh37
NC_000011.8:g.2639816A>C	NCBI36
NG_008935.1:g.222020A>C , LRG_287:g.222020A>C
NG_016178.2:g.42989T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1086A>C (KCNQ1)	ENSP00000434560.2:p.Arg362Ser
ENST00000646564.2:c.903A>C (KCNQ1)	ENSP00000495806.2:p.Arg301Ser
ENST00000155840.12:c.1443A>C (KCNQ1) MANE Select	ENSP00000155840.2:p.Arg481Ser
ENST00000335475.6:c.1062A>C (KCNQ1)	ENSP00000334497.5:p.Arg354Ser
ENST00000646564.1:c.549A>C (KCNQ1)	ENSP00000495806.1:p.Arg183Ser
ENST00000155840.9:c.1443A>C (KCNQ1)	ENSP00000155840.2:p.Arg481Ser
ENST00000335475.5:c.1062A>C (KCNQ1)	ENSP00000334497.5:p.Arg354Ser
NM_000218.2:c.1443A>C , LRG_287t1:c.1443A>C (KCNQ1)	NP_000209.2:p.Arg481Ser
NM_181798.1:c.1062A>C , LRG_287t2:c.1062A>C (KCNQ1)	NP_861463.1:p.Arg354Ser
NR_002728.3:n.37989T>G (KCNQ1OT1)
NM_000218.3:c.1443A>C (KCNQ1) MANE Select	NP_000209.2:p.Arg481Ser