Canonical Allele Identifier: CA030509

Gene: KCNQ1

Linked Data

• dbSNP Id: rs377094128
• ExAC: 11:2790048 A / C
• gnomAD v2: 11-2790048-A-C
• gnomAD v3: 11-2768818-A-C
• gnomAD v4: 11-2768818-A-C
• MyVariant Identifiers: chr11:g.2790048A>C (hg19) ; chr11:g.2768818A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768818A>C , CM000673.2:g.2768818A>C	GRCh38
NC_000011.9:g.2790048A>C , CM000673.1:g.2790048A>C	GRCh37
NC_000011.8:g.2746624A>C	NCBI36
NG_008935.1:g.328828A>C , LRG_287:g.328828A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1158-26A>C	ENSP00000434560.2:n.1158-26A>C
ENST00000646564.2:c.975-26A>C	ENSP00000495806.2:n.975-26A>C
ENST00000155840.12:c.1515-26A>C MANE Select	ENSP00000155840.2:n.1515-26A>C
ENST00000335475.6:c.1134-26A>C	ENSP00000334497.5:n.1134-26A>C
ENST00000646564.1:c.621-26A>C	ENSP00000495806.1:n.621-26A>C
ENST00000155840.9:c.1515-26A>C	ENSP00000155840.2:n.1515-26A>C
ENST00000335475.5:c.1134-26A>C	ENSP00000334497.5:n.1134-26A>C
NM_000218.2:c.1515-26A>C , LRG_287t1:c.1515-26A>C	NP_000209.2:n.1515-26A>C
NM_181798.1:c.1134-26A>C , LRG_287t2:c.1134-26A>C	NP_861463.1:n.1134-26A>C
NM_000218.3:c.1515-26A>C MANE Select	NP_000209.2:n.1515-26A>C