Canonical Allele Identifier: CA379131482

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2594136T>A (hg19) ; chr11:g.2572906T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572906T>A , CM000673.2:g.2572906T>A	GRCh38
NC_000011.9:g.2594136T>A , CM000673.1:g.2594136T>A	GRCh37
NC_000011.8:g.2550712T>A	NCBI36
NG_008935.1:g.132916T>A , LRG_287:g.132916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.580T>A	ENSP00000434560.2:p.Tyr194Asn
ENST00000646564.2:c.478-10529T>A	ENSP00000495806.2:n.478-10529T>A
ENST00000155840.12:c.841T>A MANE Select	ENSP00000155840.2:p.Tyr281Asn
ENST00000335475.6:c.460T>A	ENSP00000334497.5:p.Tyr154Asn
ENST00000646564.1:c.124-10529T>A	ENSP00000495806.1:n.124-10529T>A
ENST00000155840.9:c.841T>A	ENSP00000155840.2:p.Tyr281Asn
ENST00000335475.5:c.460T>A	ENSP00000334497.5:p.Tyr154Asn
ENST00000496887.6:c.580T>A
NM_000218.2:c.841T>A , LRG_287t1:c.841T>A	NP_000209.2:p.Tyr281Asn
NM_181798.1:c.460T>A , LRG_287t2:c.460T>A	NP_861463.1:p.Tyr154Asn
NM_000218.3:c.841T>A MANE Select	NP_000209.2:p.Tyr281Asn