Canonical Allele Identifier: CA653929409

Gene: KCNQ1

Linked Data

• COSMIC: COSN1131064

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2571664C>T , CM000673.2:g.2571664C>T	GRCh38
NC_000011.9:g.2592894C>T , CM000673.1:g.2592894C>T	GRCh37
NC_000011.8:g.2549470C>T	NCBI36
NG_008935.1:g.131674C>T , LRG_287:g.131674C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.422+261C>T	ENSP00000434560.2:n.422+261C>T
ENST00000646564.2:c.478-11771C>T	ENSP00000495806.2:n.478-11771C>T
ENST00000155840.12:c.683+261C>T MANE Select	ENSP00000155840.2:n.683+261C>T
ENST00000335475.6:c.302+261C>T	ENSP00000334497.5:n.302+261C>T
ENST00000646564.1:c.124-11771C>T	ENSP00000495806.1:n.124-11771C>T
ENST00000155840.9:c.683+261C>T	ENSP00000155840.2:n.683+261C>T
ENST00000335475.5:c.302+261C>T	ENSP00000334497.5:n.302+261C>T
ENST00000496887.6:c.422+261C>T	ENSP00000434560.1:n.422+261C>T
NM_000218.2:c.683+261C>T , LRG_287t1:c.683+261C>T	NP_000209.2:n.683+261C>T
NM_181798.1:c.302+261C>T , LRG_287t2:c.302+261C>T	NP_861463.1:n.302+261C>T
NM_000218.3:c.683+261C>T MANE Select	NP_000209.2:n.683+261C>T