Canonical Allele Identifier: CA2259200789
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665873C= , CM000679.2:g.39665873C= GRCh38
NC_000017.10:g.37822126C= , CM000679.1:g.37822126C= GRCh37
NC_000017.9:g.35075652C= NCBI36
NG_008892.1:g.5528C= , LRG_210:g.5528C=
NG_042278.1:g.2893C=

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.268C= MANE Select ENSP00000312624.2:p.Pro90=
ENST00000309889.2:c.268C= ENSP00000312624.2:p.Pro90=
ENST00000578283.1:c.196C= ENSP00000462787.1:p.Pro66=
NM_003673.3:c.268C= , LRG_210t1:c.268C= NP_003664.1:p.Pro90=
NM_003673.4:c.268C= MANE Select NP_003664.1:p.Pro90=