Canonical Allele Identifier: CA2637631359
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664951del , CM000679.2:g.39664951del GRCh38
NC_000017.10:g.37821204del , CM000679.1:g.37821204del GRCh37
NC_000017.9:g.35074730del NCBI36
NG_008892.1:g.4606del , LRG_210:g.4606del
NG_042278.1:g.1971del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-409del ENSP00000312624.2:n.-409del