Canonical Allele Identifier: CA117570
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 5526
dbSNP Id: rs786205076

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665469_39665470del , CM000679.2:g.39665469_39665470del GRCh38
NC_000017.10:g.37821722_37821723del , CM000679.1:g.37821722_37821723del GRCh37
NC_000017.9:g.35075248_35075249del NCBI36
NG_008892.1:g.5124_5125del , LRG_210:g.5124_5125del
NG_042278.1:g.2489_2490del

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.110_110+1del
ENST00000309889.2:c.110_110+1del
ENST00000578283.1:c.110_110+1del
NM_003673.3:c.110_110+1del , LRG_210t1:c.110_110+1del
NM_003673.4:c.110_110+1del