Canonical Allele Identifier: CA597114435

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• dbSNP Id: rs1168072539
• gnomAD v2: 11-2869643-C-A
• gnomAD v4: 11-2848413-C-A
• MyVariant Identifiers: chr11:g.2869643C>A (hg19) ; chr11:g.2848413C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848413C>A , CM000673.2:g.2848413C>A	GRCh38
NC_000011.9:g.2869643C>A , CM000673.1:g.2869643C>A	GRCh37
NC_000011.8:g.2826219C>A	NCBI36
NG_008935.1:g.408423C>A , LRG_287:g.408423C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.*410C>A (KCNQ1)	ENSP00000434560.2:n.*410C>A
ENST00000155840.12:c.*410C>A (KCNQ1) MANE Select	ENSP00000155840.2:n.*410C>A
ENST00000335475.6:c.*410C>A (KCNQ1)	ENSP00000334497.5:n.*410C>A
ENST00000155840.9:c.*410C>A (KCNQ1)	ENSP00000155840.2:n.*410C>A
ENST00000526095.1:n.948C>A (KCNQ1)
NM_000218.2:c.*410C>A , LRG_287t1:c.*410C>A (KCNQ1)	NP_000209.2:n.*410C>A
NM_181798.1:c.*410C>A , LRG_287t2:c.*410C>A (KCNQ1)	NP_861463.1:n.*410C>A
NR_130721.1:n.778-7971G>T (KCNQ1-AS1)
NM_000218.3:c.*410C>A (KCNQ1) MANE Select	NP_000209.2:n.*410C>A