Canonical Allele Identifier: CA2637632293
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665576_39665582del , CM000679.2:g.39665576_39665582del GRCh38
NC_000017.10:g.37821829_37821835del , CM000679.1:g.37821829_37821835del GRCh37
NC_000017.9:g.35075355_35075361del NCBI36
NG_008892.1:g.5231_5237del , LRG_210:g.5231_5237del
NG_042278.1:g.2596_2602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.110+107_110+113del MANE Select ENSP00000312624.2:n.110+107_110+113del
ENST00000309889.2:c.110+107_110+113del ENSP00000312624.2:n.110+107_110+113del
ENST00000578283.1:c.110+107_110+113del ENSP00000462787.1:n.110+107_110+113del
NM_003673.3:c.110+107_110+113del , LRG_210t1:c.110+107_110+113del NP_003664.1:n.110+107_110+113del
NM_003673.4:c.110+107_110+113del MANE Select NP_003664.1:n.110+107_110+113del