Canonical Allele Identifier: CA2637632987
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665971-CCTGGGTGGCCA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665972_39665982del , CM000679.2:g.39665972_39665982del GRCh38
NC_000017.10:g.37822225_37822235del , CM000679.1:g.37822225_37822235del GRCh37
NC_000017.9:g.35075751_35075761del NCBI36
NG_008892.1:g.5627_5637del , LRG_210:g.5627_5637del
NG_042278.1:g.2992_3002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.367_377del MANE Select ENSP00000312624.2:p.Leu123ValfsTer9
ENST00000309889.2:c.367_377del ENSP00000312624.2:p.Leu123ValfsTer9
ENST00000578283.1:c.295_305del ENSP00000462787.1:p.Leu99ValfsTer9
NM_003673.3:c.367_377del , LRG_210t1:c.367_377del NP_003664.1:p.Leu123ValfsTer9
NM_003673.4:c.367_377del MANE Select NP_003664.1:p.Leu123ValfsTer9
Search 100 bp 5'
Search 100 bp 3'