Canonical Allele Identifier: CA2637631825

Gene: TCAP

Linked Data

• gnomAD v4: 17-39665172-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665175_39665176del , CM000679.2:g.39665175_39665176del	GRCh38
NC_000017.10:g.37821428_37821429del , CM000679.1:g.37821428_37821429del	GRCh37
NC_000017.9:g.35074954_35074955del	NCBI36
NG_008892.1:g.4830_4831del , LRG_210:g.4830_4831del
NG_042278.1:g.2195_2196del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-185_-184del	ENSP00000312624.2:n.-185_-184del