Canonical Allele Identifier: CA379133060

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604734T>A (hg19) ; chr11:g.2583504T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583504T>A , CM000673.2:g.2583504T>A	GRCh38
NC_000011.9:g.2604734T>A , CM000673.1:g.2604734T>A	GRCh37
NC_000011.8:g.2561310T>A	NCBI36
NG_008935.1:g.143514T>A , LRG_287:g.143514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.730T>A	ENSP00000434560.2:p.Cys244Ser
ENST00000646564.2:c.547T>A	ENSP00000495806.2:p.Cys183Ser
ENST00000155840.12:c.991T>A MANE Select	ENSP00000155840.2:p.Cys331Ser
ENST00000335475.6:c.610T>A	ENSP00000334497.5:p.Cys204Ser
ENST00000646564.1:c.193T>A	ENSP00000495806.1:p.Cys65Ser
ENST00000155840.9:c.991T>A	ENSP00000155840.2:p.Cys331Ser
ENST00000335475.5:c.610T>A	ENSP00000334497.5:p.Cys204Ser
NM_000218.2:c.991T>A , LRG_287t1:c.991T>A	NP_000209.2:p.Cys331Ser
NM_181798.1:c.610T>A , LRG_287t2:c.610T>A	NP_861463.1:p.Cys204Ser
NM_000218.3:c.991T>A MANE Select	NP_000209.2:p.Cys331Ser