Canonical Allele Identifier: CA2637632160
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665395-G-GGAGAACTGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665399_39665407dup , CM000679.2:g.39665399_39665407dup GRCh38
NC_000017.10:g.37821652_37821660dup , CM000679.1:g.37821652_37821660dup GRCh37
NC_000017.9:g.35075178_35075186dup NCBI36
NG_008892.1:g.5054_5062dup , LRG_210:g.5054_5062dup
NG_042278.1:g.2419_2427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.40_48dup MANE Select ENSP00000312624.2:p.Glu16_Arg17insAsnCysGlu
ENST00000309889.2:c.40_48dup ENSP00000312624.2:p.Glu16_Arg17insAsnCysGlu
ENST00000578283.1:c.40_48dup ENSP00000462787.1:p.Glu16_Arg17insAsnCysGlu
NM_003673.3:c.40_48dup , LRG_210t1:c.40_48dup NP_003664.1:p.Glu16_Arg17insAsnCysGlu
NM_003673.4:c.40_48dup MANE Select NP_003664.1:p.Glu16_Arg17insAsnCysGlu
Search 100 bp 5'
Search 100 bp 3'