Canonical Allele Identifier: CA379140389

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• gnomAD v4: 11-2847872-G-A
• MyVariant Identifiers: chr11:g.2869102G>A (hg19) ; chr11:g.2847872G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2847872G>A , CM000673.2:g.2847872G>A	GRCh38
NC_000011.9:g.2869102G>A , CM000673.1:g.2869102G>A	GRCh37
NC_000011.8:g.2825678G>A	NCBI36
NG_008935.1:g.407882G>A , LRG_287:g.407882G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1543G>A (KCNQ1)	ENSP00000434560.2:p.Gly515Ser
ENST00000155840.12:c.1900G>A (KCNQ1) MANE Select	ENSP00000155840.2:p.Gly634Ser
ENST00000335475.6:c.1519G>A (KCNQ1)	ENSP00000334497.5:p.Gly507Ser
ENST00000526095.2:c.304G>A (KCNQ1)	ENSP00000494939.1:p.Gly102Ser
ENST00000155840.9:c.1900G>A (KCNQ1)	ENSP00000155840.2:p.Gly634Ser
ENST00000335475.5:c.1519G>A (KCNQ1)	ENSP00000334497.5:p.Gly507Ser
ENST00000526095.1:n.407G>A (KCNQ1)
NM_000218.2:c.1900G>A , LRG_287t1:c.1900G>A (KCNQ1)	NP_000209.2:p.Gly634Ser
NM_181798.1:c.1519G>A , LRG_287t2:c.1519G>A (KCNQ1)	NP_861463.1:p.Gly507Ser
NR_130721.1:n.778-7430C>T (KCNQ1-AS1)
NM_000218.3:c.1900G>A (KCNQ1) MANE Select	NP_000209.2:p.Gly634Ser