Canonical Allele Identifier: CA379140222

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• MyVariant Identifiers: chr11:g.2869019T>G (hg19) ; chr11:g.2847789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2847789T>G , CM000673.2:g.2847789T>G	GRCh38
NC_000011.9:g.2869019T>G , CM000673.1:g.2869019T>G	GRCh37
NC_000011.8:g.2825595T>G	NCBI36
NG_008935.1:g.407799T>G , LRG_287:g.407799T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1460T>G (KCNQ1)	ENSP00000434560.2:p.Leu487Arg
ENST00000155840.12:c.1817T>G (KCNQ1) MANE Select	ENSP00000155840.2:p.Leu606Arg
ENST00000335475.6:c.1436T>G (KCNQ1)	ENSP00000334497.5:p.Leu479Arg
ENST00000526095.2:c.221T>G (KCNQ1)	ENSP00000494939.1:p.Leu74Arg
ENST00000155840.9:c.1817T>G (KCNQ1)	ENSP00000155840.2:p.Leu606Arg
ENST00000335475.5:c.1436T>G (KCNQ1)	ENSP00000334497.5:p.Leu479Arg
ENST00000526095.1:n.324T>G (KCNQ1)
NM_000218.2:c.1817T>G , LRG_287t1:c.1817T>G (KCNQ1)	NP_000209.2:p.Leu606Arg
NM_181798.1:c.1436T>G , LRG_287t2:c.1436T>G (KCNQ1)	NP_861463.1:p.Leu479Arg
NR_130721.1:n.778-7347A>C (KCNQ1-AS1)
NM_000218.3:c.1817T>G (KCNQ1) MANE Select	NP_000209.2:p.Leu606Arg