Canonical Allele Identifier: CA379479588

Gene: KCNQ1 KCNQ1OT1

Linked Data

• MyVariant Identifiers: chr11:g.2683250T>C (hg19) ; chr11:g.2662020T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662020T>C , CM000673.2:g.2662020T>C	GRCh38
NC_000011.9:g.2683250T>C , CM000673.1:g.2683250T>C	GRCh37
NC_000011.8:g.2639826T>C	NCBI36
NG_008935.1:g.222030T>C , LRG_287:g.222030T>C
NG_016178.2:g.42979A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1096T>C (KCNQ1)	ENSP00000434560.2:p.Phe366Leu
ENST00000646564.2:c.913T>C (KCNQ1)	ENSP00000495806.2:p.Phe305Leu
ENST00000155840.12:c.1453T>C (KCNQ1) MANE Select	ENSP00000155840.2:p.Phe485Leu
ENST00000335475.6:c.1072T>C (KCNQ1)	ENSP00000334497.5:p.Phe358Leu
ENST00000646564.1:c.559T>C (KCNQ1)	ENSP00000495806.1:p.Phe187Leu
ENST00000155840.9:c.1453T>C (KCNQ1)	ENSP00000155840.2:p.Phe485Leu
ENST00000335475.5:c.1072T>C (KCNQ1)	ENSP00000334497.5:p.Phe358Leu
NM_000218.2:c.1453T>C , LRG_287t1:c.1453T>C (KCNQ1)	NP_000209.2:p.Phe485Leu
NM_181798.1:c.1072T>C , LRG_287t2:c.1072T>C (KCNQ1)	NP_861463.1:p.Phe358Leu
NR_002728.3:n.37979A>G (KCNQ1OT1)
NM_000218.3:c.1453T>C (KCNQ1) MANE Select	NP_000209.2:p.Phe485Leu