Canonical Allele Identifier: CA2259200477
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665338_39665340delinsGGA , CM000679.2:g.39665338_39665340delinsGGA GRCh38
NC_000017.10:g.37821591_37821593delinsGGA , CM000679.1:g.37821591_37821593delinsGGA GRCh37
NC_000017.9:g.35075117_35075119delinsGGA NCBI36
NG_008892.1:g.4993_4995delinsGGA , LRG_210:g.4993_4995delinsGGA
NG_042278.1:g.2358_2360delinsGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-22_-20delinsGGA ENSP00000312624.2:n.-22_-20delinsGGA