Canonical Allele Identifier: CA379121386

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549195C>A (hg19) ; chr11:g.2527965C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527965C>A , CM000673.2:g.2527965C>A	GRCh38
NC_000011.9:g.2549195C>A , CM000673.1:g.2549195C>A	GRCh37
NC_000011.8:g.2505771C>A	NCBI36
NG_008935.1:g.87975C>A , LRG_287:g.87975C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.221C>A
ENST00000496887.7:c.163C>A	ENSP00000434560.2:p.Leu55Met
ENST00000646564.2:c.424C>A	ENSP00000495806.2:p.Leu142Met
ENST00000155840.12:c.424C>A MANE Select	ENSP00000155840.2:p.Leu142Met
ENST00000335475.6:c.43C>A	ENSP00000334497.5:p.Leu15Met
ENST00000646564.1:c.70C>A	ENSP00000495806.1:p.Leu24Met
ENST00000155840.9:c.424C>A	ENSP00000155840.2:p.Leu142Met
ENST00000335475.5:c.43C>A	ENSP00000334497.5:p.Leu15Met
ENST00000345015.4:n.293C>A
ENST00000380776.4:c.214C>A	ENSP00000370153.4:p.Leu72Met
ENST00000496887.6:c.163C>A	ENSP00000434560.1:p.Leu55Met
NM_000218.2:c.424C>A , LRG_287t1:c.424C>A	NP_000209.2:p.Leu142Met
NM_181798.1:c.43C>A , LRG_287t2:c.43C>A	NP_861463.1:p.Leu15Met
NM_000218.3:c.424C>A MANE Select	NP_000209.2:p.Leu142Met