Canonical Allele Identifier: CA771858472
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1256226165
MyVariant Identifiers: chr17:g.37822219del (hg19) chr17:g.39665966del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665966del , CM000679.2:g.39665966del GRCh38
NC_000017.10:g.37822219del , CM000679.1:g.37822219del GRCh37
NC_000017.9:g.35075745del NCBI36
NG_008892.1:g.5621del , LRG_210:g.5621del
NG_042278.1:g.2986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.361del MANE Select ENSP00000312624.2:p.Thr121GlnfsTer?
ENST00000309889.2:c.361del ENSP00000312624.2:p.Thr121GlnfsTer?
ENST00000578283.1:c.289del ENSP00000462787.1:p.Thr97GlnfsTer?
NM_003673.3:c.361del , LRG_210t1:c.361del NP_003664.1:p.Thr121GlnfsTer?
NM_003673.4:c.361del MANE Select NP_003664.1:p.Thr121GlnfsTer?
Search 100 bp 5'
Search 100 bp 3'