Canonical Allele Identifier: CA379134759

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2608858T>C (hg19) ; chr11:g.2587628T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587628T>C , CM000673.2:g.2587628T>C	GRCh38
NC_000011.9:g.2608858T>C , CM000673.1:g.2608858T>C	GRCh37
NC_000011.8:g.2565434T>C	NCBI36
NG_008935.1:g.147638T>C , LRG_287:g.147638T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.830T>C	ENSP00000434560.2:p.Ile277Thr
ENST00000646564.2:c.647T>C	ENSP00000495806.2:p.Ile216Thr
ENST00000155840.12:c.1187T>C MANE Select	ENSP00000155840.2:p.Ile396Thr
ENST00000335475.6:c.806T>C	ENSP00000334497.5:p.Ile269Thr
ENST00000646564.1:c.293T>C	ENSP00000495806.1:p.Ile98Thr
ENST00000155840.9:c.1187T>C	ENSP00000155840.2:p.Ile396Thr
ENST00000335475.5:c.806T>C	ENSP00000334497.5:p.Ile269Thr
NM_000218.2:c.1187T>C , LRG_287t1:c.1187T>C	NP_000209.2:p.Ile396Thr
NM_181798.1:c.806T>C , LRG_287t2:c.806T>C	NP_861463.1:p.Ile269Thr
NM_000218.3:c.1187T>C MANE Select	NP_000209.2:p.Ile396Thr