Canonical Allele Identifier: CA2637632313

Gene: TCAP

Linked Data

• gnomAD v4: 17-39665590-TGGGGAGAGCAAAGGGGAACCACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665591_39665613del , CM000679.2:g.39665591_39665613del	GRCh38
NC_000017.10:g.37821844_37821866del , CM000679.1:g.37821844_37821866del	GRCh37
NC_000017.9:g.35075370_35075392del	NCBI36
NG_008892.1:g.5246_5268del , LRG_210:g.5246_5268del
NG_042278.1:g.2611_2633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.110+122_111-103del MANE Select	ENSP00000312624.2:n.110+122_111-103del
ENST00000309889.2:c.110+122_111-103del	ENSP00000312624.2:n.110+122_111-103del
ENST00000578283.1:c.110+122_111-103del	ENSP00000462787.1:n.110+122_111-103del
NM_003673.3:c.110+122_111-103del , LRG_210t1:c.110+122_111-103del	NP_003664.1:n.110+122_111-103del
NM_003673.4:c.110+122_111-103del MANE Select	NP_003664.1:n.110+122_111-103del