Canonical Allele Identifier: CA2790208898

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2828109C>G , CM000673.2:g.2828109C>G	GRCh38
NC_000011.9:g.2849339C>G , CM000673.1:g.2849339C>G	GRCh37
NC_000011.8:g.2805915C>G	NCBI36
NG_008935.1:g.388119C>G , LRG_287:g.388119C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1438-19658C>G	ENSP00000434560.2:n.1438-19658C>G
ENST00000646564.2:c.1255-11607C>G	ENSP00000495806.2:n.1255-11607C>G
ENST00000155840.12:c.1795-19658C>G MANE Select	ENSP00000155840.2:n.1795-19658C>G
ENST00000335475.6:c.1414-19658C>G	ENSP00000334497.5:n.1414-19658C>G
ENST00000526095.2:c.199-19658C>G	ENSP00000494939.1:n.199-19658C>G
ENST00000646564.1:c.901-11607C>G	ENSP00000495806.1:n.901-11607C>G
ENST00000155840.9:c.1795-19658C>G	ENSP00000155840.2:n.1795-19658C>G
ENST00000335475.5:c.1414-19658C>G	ENSP00000334497.5:n.1414-19658C>G
ENST00000526095.1:n.302-19658C>G
NM_000218.2:c.1795-19658C>G , LRG_287t1:c.1795-19658C>G	NP_000209.2:n.1795-19658C>G
NM_181798.1:c.1414-19658C>G , LRG_287t2:c.1414-19658C>G	NP_861463.1:n.1414-19658C>G
NM_000218.3:c.1795-19658C>G MANE Select	NP_000209.2:n.1795-19658C>G