Canonical Allele Identifier: CA216346397

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• dbSNP Id: rs772946233
• MyVariant Identifiers: chr11:g.2870077A>G (hg19) ; chr11:g.2848847A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848847A>G , CM000673.2:g.2848847A>G	GRCh38
NC_000011.9:g.2870077A>G , CM000673.1:g.2870077A>G	GRCh37
NC_000011.8:g.2826653A>G	NCBI36
NG_008935.1:g.408857A>G , LRG_287:g.408857A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.*844A>G (KCNQ1)	ENSP00000434560.2:n.*844A>G
ENST00000155840.12:c.*844A>G (KCNQ1) MANE Select	ENSP00000155840.2:n.*844A>G
ENST00000335475.6:c.*844A>G (KCNQ1)	ENSP00000334497.5:n.*844A>G
ENST00000155840.9:c.*844A>G (KCNQ1)	ENSP00000155840.2:n.*844A>G
NM_000218.2:c.*844A>G , LRG_287t1:c.*844A>G (KCNQ1)	NP_000209.2:n.*844A>G
NM_181798.1:c.*844A>G , LRG_287t2:c.*844A>G (KCNQ1)	NP_861463.1:n.*844A>G
NR_130721.1:n.778-8405T>C (KCNQ1-AS1)
NM_000218.3:c.*844A>G (KCNQ1) MANE Select	NP_000209.2:n.*844A>G