Canonical Allele Identifier: CA2740093574
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2971269
ClinVar RCV Id: RCV003827451

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587566_2587592del , CM000673.2:g.2587566_2587592del GRCh38
NC_000011.9:g.2608796_2608822del , CM000673.1:g.2608796_2608822del GRCh37
NC_000011.8:g.2565372_2565398del NCBI36
NG_008935.1:g.147576_147602del , LRG_287:g.147576_147602del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.772-4_794del
ENST00000646564.2:c.589-4_611del
ENST00000155840.12:c.1129-4_1151del
ENST00000335475.6:c.748-4_770del
ENST00000646564.1:c.235-4_257del
ENST00000155840.9:c.1129-4_1151del
ENST00000335475.5:c.748-4_770del
NM_000218.2:c.1129-4_1151del , LRG_287t1:c.1129-4_1151del
NM_181798.1:c.748-4_770del , LRG_287t2:c.748-4_770del
NM_000218.3:c.1129-4_1151del