Canonical Allele Identifier: CA472415613

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2445122-C-T
• MyVariant Identifiers: chr11:g.2466352C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2445122C>T , CM000673.2:g.2445122C>T	GRCh38
NC_000011.9:g.2466352C>T , CM000673.1:g.2466352C>T	GRCh37
NC_000011.8:g.2422928C>T	NCBI36
NG_008935.1:g.5132C>T , LRG_287:g.5132C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.24-261C>T	ENSP00000434560.2:n.24-261C>T
ENST00000646564.2:c.24C>T	ENSP00000495806.2:p.Pro8=
ENST00000155840.12:c.24C>T MANE Select	ENSP00000155840.2:p.Pro8=
ENST00000155840.9:c.24C>T	ENSP00000155840.2:p.Pro8=
ENST00000496887.6:c.24-261C>T	ENSP00000434560.1:n.24-261C>T
NM_000218.2:c.24C>T , LRG_287t1:c.24C>T	NP_000209.2:p.Pro8=
NM_000218.3:c.24C>T MANE Select	NP_000209.2:p.Pro8=