Canonical Allele Identifier: CA2637632080
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665301_39665313del , CM000679.2:g.39665301_39665313del GRCh38
NC_000017.10:g.37821554_37821566del , CM000679.1:g.37821554_37821566del GRCh37
NC_000017.9:g.35075080_35075092del NCBI36
NG_008892.1:g.4956_4968del , LRG_210:g.4956_4968del
NG_042278.1:g.2321_2333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-59_-47del ENSP00000312624.2:n.-59_-47del