Canonical Allele Identifier: CA379133103

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604753T>C (hg19) ; chr11:g.2583523T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583523T>C , CM000673.2:g.2583523T>C	GRCh38
NC_000011.9:g.2604753T>C , CM000673.1:g.2604753T>C	GRCh37
NC_000011.8:g.2561329T>C	NCBI36
NG_008935.1:g.143533T>C , LRG_287:g.143533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.749T>C	ENSP00000434560.2:p.Ile250Thr
ENST00000646564.2:c.566T>C	ENSP00000495806.2:p.Ile189Thr
ENST00000155840.12:c.1010T>C MANE Select	ENSP00000155840.2:p.Ile337Thr
ENST00000335475.6:c.629T>C	ENSP00000334497.5:p.Ile210Thr
ENST00000646564.1:c.212T>C	ENSP00000495806.1:p.Ile71Thr
ENST00000155840.9:c.1010T>C	ENSP00000155840.2:p.Ile337Thr
ENST00000335475.5:c.629T>C	ENSP00000334497.5:p.Ile210Thr
NM_000218.2:c.1010T>C , LRG_287t1:c.1010T>C	NP_000209.2:p.Ile337Thr
NM_181798.1:c.629T>C , LRG_287t2:c.629T>C	NP_861463.1:p.Ile210Thr
NM_000218.3:c.1010T>C MANE Select	NP_000209.2:p.Ile337Thr