Canonical Allele Identifier: CA2637632115
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665335del , CM000679.2:g.39665335del GRCh38
NC_000017.10:g.37821588del , CM000679.1:g.37821588del GRCh37
NC_000017.9:g.35075114del NCBI36
NG_008892.1:g.4990del , LRG_210:g.4990del
NG_042278.1:g.2355del

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-25del ENSP00000312624.2:n.-25del