Canonical Allele Identifier: CA2637632328
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665600-AAAGGGGAACCACCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665601_39665614del , CM000679.2:g.39665601_39665614del GRCh38
NC_000017.10:g.37821854_37821867del , CM000679.1:g.37821854_37821867del GRCh37
NC_000017.9:g.35075380_35075393del NCBI36
NG_008892.1:g.5256_5269del , LRG_210:g.5256_5269del
NG_042278.1:g.2621_2634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.111-115_111-102del MANE Select ENSP00000312624.2:n.111-115_111-102del
ENST00000309889.2:c.111-115_111-102del ENSP00000312624.2:n.111-115_111-102del
ENST00000578283.1:c.111-115_111-102del ENSP00000462787.1:n.111-115_111-102del
NM_003673.3:c.111-115_111-102del , LRG_210t1:c.111-115_111-102del NP_003664.1:n.111-115_111-102del
NM_003673.4:c.111-115_111-102del MANE Select NP_003664.1:n.111-115_111-102del
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