Canonical Allele Identifier: CA379133006

Gene: KCNQ1

Linked Data

• dbSNP Id: rs794728518
• MyVariant Identifiers: chr11:g.2604705A>T (hg19) ; chr11:g.2583475A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583475A>T , CM000673.2:g.2583475A>T	GRCh38
NC_000011.9:g.2604705A>T , CM000673.1:g.2604705A>T	GRCh37
NC_000011.8:g.2561281A>T	NCBI36
NG_008935.1:g.143485A>T , LRG_287:g.143485A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.701A>T	ENSP00000434560.2:p.Gln234Leu
ENST00000646564.2:c.518A>T	ENSP00000495806.2:p.Gln173Leu
ENST00000155840.12:c.962A>T MANE Select	ENSP00000155840.2:p.Gln321Leu
ENST00000335475.6:c.581A>T	ENSP00000334497.5:p.Gln194Leu
ENST00000646564.1:c.164A>T	ENSP00000495806.1:p.Gln55Leu
ENST00000155840.9:c.962A>T	ENSP00000155840.2:p.Gln321Leu
ENST00000335475.5:c.581A>T	ENSP00000334497.5:p.Gln194Leu
NM_000218.2:c.962A>T , LRG_287t1:c.962A>T	NP_000209.2:p.Gln321Leu
NM_181798.1:c.581A>T , LRG_287t2:c.581A>T	NP_861463.1:p.Gln194Leu
NM_000218.3:c.962A>T MANE Select	NP_000209.2:p.Gln321Leu