Canonical Allele Identifier: CA216332363

Gene: KCNQ1

Linked Data

• dbSNP Id: rs915646669
• gnomAD v2: 11-2608723-G-A
• gnomAD v3: 11-2587493-G-A
• gnomAD v4: 11-2587493-G-A
• MyVariant Identifiers: chr11:g.2608723G>A (hg19) ; chr11:g.2587493G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587493G>A , CM000673.2:g.2587493G>A	GRCh38
NC_000011.9:g.2608723G>A , CM000673.1:g.2608723G>A	GRCh37
NC_000011.8:g.2565299G>A	NCBI36
NG_008935.1:g.147503G>A , LRG_287:g.147503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.772-77G>A	ENSP00000434560.2:n.772-77G>A
ENST00000646564.2:c.589-77G>A	ENSP00000495806.2:n.589-77G>A
ENST00000155840.12:c.1129-77G>A MANE Select	ENSP00000155840.2:n.1129-77G>A
ENST00000335475.6:c.748-77G>A	ENSP00000334497.5:n.748-77G>A
ENST00000646564.1:c.235-77G>A	ENSP00000495806.1:n.235-77G>A
ENST00000155840.9:c.1129-77G>A	ENSP00000155840.2:n.1129-77G>A
ENST00000335475.5:c.748-77G>A	ENSP00000334497.5:n.748-77G>A
NM_000218.2:c.1129-77G>A , LRG_287t1:c.1129-77G>A	NP_000209.2:n.1129-77G>A
NM_181798.1:c.748-77G>A , LRG_287t2:c.748-77G>A	NP_861463.1:n.748-77G>A
NM_000218.3:c.1129-77G>A MANE Select	NP_000209.2:n.1129-77G>A