Canonical Allele Identifier: CA2259200725

Gene: TCAP

Linked Data

• dbSNP Id: rs2057248838
• gnomAD v4: 17-39665620-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665625del , CM000679.2:g.39665625del	GRCh38
NC_000017.10:g.37821878del , CM000679.1:g.37821878del	GRCh37
NC_000017.9:g.35075404del	NCBI36
NG_008892.1:g.5280del , LRG_210:g.5280del
NG_042278.1:g.2645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.111-91del MANE Select	ENSP00000312624.2:n.111-91del
ENST00000309889.2:c.111-91del	ENSP00000312624.2:n.111-91del
ENST00000578283.1:c.111-91del	ENSP00000462787.1:n.111-91del
NM_003673.3:c.111-91del , LRG_210t1:c.111-91del	NP_003664.1:n.111-91del
NM_003673.4:c.111-91del MANE Select	NP_003664.1:n.111-91del