Canonical Allele Identifier: CA2637631992
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665243_39665246del , CM000679.2:g.39665243_39665246del GRCh38
NC_000017.10:g.37821496_37821499del , CM000679.1:g.37821496_37821499del GRCh37
NC_000017.9:g.35075022_35075025del NCBI36
NG_008892.1:g.4898_4901del , LRG_210:g.4898_4901del
NG_042278.1:g.2263_2266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-117_-114del ENSP00000312624.2:n.-117_-114del