Canonical Allele Identifier: CA2637632837

Gene: TCAP

Linked Data

• gnomAD v4: 17-39665901-TGGGCGCCACCAAGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665903_39665918del , CM000679.2:g.39665903_39665918del	GRCh38
NC_000017.10:g.37822156_37822171del , CM000679.1:g.37822156_37822171del	GRCh37
NC_000017.9:g.35075682_35075697del	NCBI36
NG_008892.1:g.5558_5573del , LRG_210:g.5558_5573del
NG_042278.1:g.2923_2938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.298_313del MANE Select	ENSP00000312624.2:p.Gly100SerfsTer?
ENST00000309889.2:c.298_313del	ENSP00000312624.2:p.Gly100SerfsTer?
ENST00000578283.1:c.226_241del	ENSP00000462787.1:p.Gly76SerfsTer?
NM_003673.3:c.298_313del , LRG_210t1:c.298_313del	NP_003664.1:p.Gly100SerfsTer?
NM_003673.4:c.298_313del MANE Select	NP_003664.1:p.Gly100SerfsTer?