Canonical Allele Identifier: CA472467371

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• MyVariant Identifiers: chr11:g.2869218C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2847988C>G , CM000673.2:g.2847988C>G	GRCh38
NC_000011.9:g.2869218C>G , CM000673.1:g.2869218C>G	GRCh37
NC_000011.8:g.2825794C>G	NCBI36
NG_008935.1:g.407998C>G , LRG_287:g.407998C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1659C>G (KCNQ1)	ENSP00000434560.2:p.Pro553=
ENST00000155840.12:c.2016C>G (KCNQ1) MANE Select	ENSP00000155840.2:p.Pro672=
ENST00000335475.6:c.1635C>G (KCNQ1)	ENSP00000334497.5:p.Pro545=
ENST00000526095.2:c.420C>G (KCNQ1)	ENSP00000494939.1:p.Pro140=
ENST00000155840.9:c.2016C>G (KCNQ1)	ENSP00000155840.2:p.Pro672=
ENST00000335475.5:c.1635C>G (KCNQ1)	ENSP00000334497.5:p.Pro545=
ENST00000526095.1:n.523C>G (KCNQ1)
NM_000218.2:c.2016C>G , LRG_287t1:c.2016C>G (KCNQ1)	NP_000209.2:p.Pro672=
NM_181798.1:c.1635C>G , LRG_287t2:c.1635C>G (KCNQ1)	NP_861463.1:p.Pro545=
NR_130721.1:n.778-7546G>C (KCNQ1-AS1)
NM_000218.3:c.2016C>G (KCNQ1) MANE Select	NP_000209.2:p.Pro672=