Canonical Allele Identifier: CA2580613271
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2562755
ClinVar RCV Id: RCV003296748

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665469_39665470dup , CM000679.2:g.39665469_39665470dup GRCh38
NC_000017.10:g.37821722_37821723dup , CM000679.1:g.37821722_37821723dup GRCh37
NC_000017.9:g.35075248_35075249dup NCBI36
NG_008892.1:g.5124_5125dup , LRG_210:g.5124_5125dup
NG_042278.1:g.2489_2490dup

Transcript Alleles

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