Canonical Allele Identifier: CA2637633209

Gene: TCAP

Linked Data

• gnomAD v4: 17-39666049-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666052del , CM000679.2:g.39666052del	GRCh38
NC_000017.10:g.37822305del , CM000679.1:g.37822305del	GRCh37
NC_000017.9:g.35075831del	NCBI36
NG_008892.1:g.5707del , LRG_210:g.5707del
NG_042278.1:g.3072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.447del MANE Select	ENSP00000312624.2:p.Gly150ValfsTer?
ENST00000309889.2:c.447del	ENSP00000312624.2:p.Gly150ValfsTer?
ENST00000578283.1:c.375del	ENSP00000462787.1:p.Gly126ValfsTer?
NM_003673.3:c.447del , LRG_210t1:c.447del	NP_003664.1:p.Gly150ValfsTer?
NM_003673.4:c.447del MANE Select	NP_003664.1:p.Gly150ValfsTer?