Canonical Allele Identifier: CA2839901300

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665508del , CM000679.2:g.39665508del	GRCh38
NC_000017.10:g.37821761del , CM000679.1:g.37821761del	GRCh37
NC_000017.9:g.35075287del	NCBI36
NG_008892.1:g.5163del , LRG_210:g.5163del
NG_042278.1:g.2528del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.110+39del MANE Select	ENSP00000312624.2:n.110+39del
ENST00000309889.2:c.110+39del	ENSP00000312624.2:n.110+39del
ENST00000578283.1:c.110+39del	ENSP00000462787.1:n.110+39del
NM_003673.3:c.110+39del , LRG_210t1:c.110+39del	NP_003664.1:n.110+39del
NM_003673.4:c.110+39del MANE Select	NP_003664.1:n.110+39del