Canonical Allele Identifier: CA2637632101
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665320_39665323del , CM000679.2:g.39665320_39665323del GRCh38
NC_000017.10:g.37821573_37821576del , CM000679.1:g.37821573_37821576del GRCh37
NC_000017.9:g.35075099_35075102del NCBI36
NG_008892.1:g.4975_4978del , LRG_210:g.4975_4978del
NG_042278.1:g.2340_2343del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-40_-37del ENSP00000312624.2:n.-40_-37del