Canonical Allele Identifier: CA2259200240
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664896_39664898delinsACT , CM000679.2:g.39664896_39664898delinsACT GRCh38
NC_000017.10:g.37821149_37821151delinsACT , CM000679.1:g.37821149_37821151delinsACT GRCh37
NC_000017.9:g.35074675_35074677delinsACT NCBI36
NG_008892.1:g.4551_4553delinsACT , LRG_210:g.4551_4553delinsACT
NG_042278.1:g.1916_1918delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-464_-462delinsACT ENSP00000312624.2:n.-464_-462delinsACT