Canonical Allele Identifier: CA2637632017
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665260dup , CM000679.2:g.39665260dup GRCh38
NC_000017.10:g.37821513dup , CM000679.1:g.37821513dup GRCh37
NC_000017.9:g.35075039dup NCBI36
NG_008892.1:g.4915dup , LRG_210:g.4915dup
NG_042278.1:g.2280dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-100dup ENSP00000312624.2:n.-100dup