Canonical Allele Identifier: CA2259200283
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664983_39664987delinsAGGGG , CM000679.2:g.39664983_39664987delinsAGGGG GRCh38
NC_000017.10:g.37821236_37821240delinsAGGGG , CM000679.1:g.37821236_37821240delinsAGGGG GRCh37
NC_000017.9:g.35074762_35074766delinsAGGGG NCBI36
NG_008892.1:g.4638_4642delinsAGGGG , LRG_210:g.4638_4642delinsAGGGG
NG_042278.1:g.2003_2007delinsAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-377_-373delinsAGGGG ENSP00000312624.2:n.-377_-373delinsAGGGG