Canonical Allele Identifier: CA675228295

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1416158370
• gnomAD v3: 11-2828236-T-A
• gnomAD v4: 11-2828236-T-A
• MyVariant Identifiers: chr11:g.2849466T>A (hg19) ; chr11:g.2828236T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2828236T>A , CM000673.2:g.2828236T>A	GRCh38
NC_000011.9:g.2849466T>A , CM000673.1:g.2849466T>A	GRCh37
NC_000011.8:g.2806042T>A	NCBI36
NG_008935.1:g.388246T>A , LRG_287:g.388246T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1438-19531T>A	ENSP00000434560.2:n.1438-19531T>A
ENST00000646564.2:c.1255-11480T>A	ENSP00000495806.2:n.1255-11480T>A
ENST00000155840.12:c.1795-19531T>A MANE Select	ENSP00000155840.2:n.1795-19531T>A
ENST00000335475.6:c.1414-19531T>A	ENSP00000334497.5:n.1414-19531T>A
ENST00000526095.2:c.199-19531T>A	ENSP00000494939.1:n.199-19531T>A
ENST00000646564.1:c.901-11480T>A	ENSP00000495806.1:n.901-11480T>A
ENST00000155840.9:c.1795-19531T>A	ENSP00000155840.2:n.1795-19531T>A
ENST00000335475.5:c.1414-19531T>A	ENSP00000334497.5:n.1414-19531T>A
ENST00000526095.1:n.302-19531T>A
NM_000218.2:c.1795-19531T>A , LRG_287t1:c.1795-19531T>A	NP_000209.2:n.1795-19531T>A
NM_181798.1:c.1414-19531T>A , LRG_287t2:c.1414-19531T>A	NP_861463.1:n.1414-19531T>A
NM_000218.3:c.1795-19531T>A MANE Select	NP_000209.2:n.1795-19531T>A