Canonical Allele Identifier: CA597114494

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• dbSNP Id: rs1481410004
• gnomAD v2: 11-2869947-C-T
• MyVariant Identifiers: chr11:g.2869947C>T (hg19) ; chr11:g.2848717C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848717C>T , CM000673.2:g.2848717C>T	GRCh38
NC_000011.9:g.2869947C>T , CM000673.1:g.2869947C>T	GRCh37
NC_000011.8:g.2826523C>T	NCBI36
NG_008935.1:g.408727C>T , LRG_287:g.408727C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.*714C>T (KCNQ1)	ENSP00000434560.2:n.*714C>T
ENST00000155840.12:c.*714C>T (KCNQ1) MANE Select	ENSP00000155840.2:n.*714C>T
ENST00000335475.6:c.*714C>T (KCNQ1)	ENSP00000334497.5:n.*714C>T
ENST00000155840.9:c.*714C>T (KCNQ1)	ENSP00000155840.2:n.*714C>T
NM_000218.2:c.*714C>T , LRG_287t1:c.*714C>T (KCNQ1)	NP_000209.2:n.*714C>T
NM_181798.1:c.*714C>T , LRG_287t2:c.*714C>T (KCNQ1)	NP_861463.1:n.*714C>T
NR_130721.1:n.778-8275G>A (KCNQ1-AS1)
NM_000218.3:c.*714C>T (KCNQ1) MANE Select	NP_000209.2:n.*714C>T