Canonical Allele Identifier: CA2637632083
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665307dup , CM000679.2:g.39665307dup GRCh38
NC_000017.10:g.37821560dup , CM000679.1:g.37821560dup GRCh37
NC_000017.9:g.35075086dup NCBI36
NG_008892.1:g.4962dup , LRG_210:g.4962dup
NG_042278.1:g.2327dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-53dup ENSP00000312624.2:n.-53dup