Canonical Allele Identifier: CA2612002800

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2528024-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2528024T>A , CM000673.2:g.2528024T>A	GRCh38
NC_000011.9:g.2549254T>A , CM000673.1:g.2549254T>A	GRCh37
NC_000011.8:g.2505830T>A	NCBI36
NG_008935.1:g.88034T>A , LRG_287:g.88034T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.216+6T>A	ENSP00000434560.2:n.216+6T>A
ENST00000646564.2:c.477+6T>A	ENSP00000495806.2:n.477+6T>A
ENST00000155840.12:c.477+6T>A MANE Select	ENSP00000155840.2:n.477+6T>A
ENST00000335475.6:c.96+6T>A	ENSP00000334497.5:n.96+6T>A
ENST00000646564.1:c.123+6T>A	ENSP00000495806.1:n.123+6T>A
ENST00000155840.9:c.477+6T>A	ENSP00000155840.2:n.477+6T>A
ENST00000335475.5:c.96+6T>A	ENSP00000334497.5:n.96+6T>A
ENST00000496887.6:c.216+6T>A	ENSP00000434560.1:n.216+6T>A
NM_000218.2:c.477+6T>A , LRG_287t1:c.477+6T>A	NP_000209.2:n.477+6T>A
NM_181798.1:c.96+6T>A , LRG_287t2:c.96+6T>A	NP_861463.1:n.96+6T>A
NM_000218.3:c.477+6T>A MANE Select	NP_000209.2:n.477+6T>A