Canonical Allele Identifier: CA2637632742
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665858_39665881del , CM000679.2:g.39665858_39665881del GRCh38
NC_000017.10:g.37822111_37822134del , CM000679.1:g.37822111_37822134del GRCh37
NC_000017.9:g.35075637_35075660del NCBI36
NG_008892.1:g.5513_5536del , LRG_210:g.5513_5536del
NG_042278.1:g.2878_2901del

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.253_276del MANE Select ENSP00000312624.2:p.Tyr85_Pro92del
ENST00000309889.2:c.253_276del ENSP00000312624.2:p.Tyr85_Pro92del
ENST00000578283.1:c.181_204del
NM_003673.3:c.253_276del , LRG_210t1:c.253_276del NP_003664.1:p.Tyr85_Pro92del
NM_003673.4:c.253_276del MANE Select NP_003664.1:p.Tyr85_Pro92del