Canonical Allele Identifier: CA2637632657
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665797-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665800del , CM000679.2:g.39665800del GRCh38
NC_000017.10:g.37822053del , CM000679.1:g.37822053del GRCh37
NC_000017.9:g.35075579del NCBI36
NG_008892.1:g.5455del , LRG_210:g.5455del
NG_042278.1:g.2820del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.195del MANE Select ENSP00000312624.2:p.Trp66GlyfsTer2
ENST00000309889.2:c.195del ENSP00000312624.2:p.Trp66GlyfsTer2
ENST00000578283.1:c.174+21del ENSP00000462787.1:n.174+21del
NM_003673.3:c.195del , LRG_210t1:c.195del NP_003664.1:p.Trp66GlyfsTer2
NM_003673.4:c.195del MANE Select NP_003664.1:p.Trp66GlyfsTer2
Search 100 bp 5'
Search 100 bp 3'