Canonical Allele Identifier: CA2259200518
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665409_39665410delinsGC , CM000679.2:g.39665409_39665410delinsGC GRCh38
NC_000017.10:g.37821662_37821663delinsGC , CM000679.1:g.37821662_37821663delinsGC GRCh37
NC_000017.9:g.35075188_35075189delinsGC NCBI36
NG_008892.1:g.5064_5065delinsGC , LRG_210:g.5064_5065delinsGC
NG_042278.1:g.2429_2430delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.50_51delinsGC MANE Select ENSP00000312624.2:p.Arg17=
ENST00000309889.2:c.50_51delinsGC ENSP00000312624.2:p.Arg17=
ENST00000578283.1:c.50_51delinsGC ENSP00000462787.1:p.Arg17=
NM_003673.3:c.50_51delinsGC , LRG_210t1:c.50_51delinsGC NP_003664.1:p.Arg17=
NM_003673.4:c.50_51delinsGC MANE Select NP_003664.1:p.Arg17=