Canonical Allele Identifier: CA379130949

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593272T>C (hg19) ; chr11:g.2572042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572042T>C , CM000673.2:g.2572042T>C	GRCh38
NC_000011.9:g.2593272T>C , CM000673.1:g.2593272T>C	GRCh37
NC_000011.8:g.2549848T>C	NCBI36
NG_008935.1:g.132052T>C , LRG_287:g.132052T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.452T>C	ENSP00000434560.2:p.Met151Thr
ENST00000646564.2:c.478-11393T>C	ENSP00000495806.2:n.478-11393T>C
ENST00000155840.12:c.713T>C MANE Select	ENSP00000155840.2:p.Met238Thr
ENST00000335475.6:c.332T>C	ENSP00000334497.5:p.Met111Thr
ENST00000646564.1:c.124-11393T>C	ENSP00000495806.1:n.124-11393T>C
ENST00000155840.9:c.713T>C	ENSP00000155840.2:p.Met238Thr
ENST00000335475.5:c.332T>C	ENSP00000334497.5:p.Met111Thr
ENST00000496887.6:c.452T>C	ENSP00000434560.1:p.Met151Thr
NM_000218.2:c.713T>C , LRG_287t1:c.713T>C	NP_000209.2:p.Met238Thr
NM_181798.1:c.332T>C , LRG_287t2:c.332T>C	NP_861463.1:p.Met111Thr
NM_000218.3:c.713T>C MANE Select	NP_000209.2:p.Met238Thr