Canonical Allele Identifier: CA2259200222
Gene: TCAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664856_39664858delinsGCA , CM000679.2:g.39664856_39664858delinsGCA GRCh38
NC_000017.10:g.37821109_37821111delinsGCA , CM000679.1:g.37821109_37821111delinsGCA GRCh37
NC_000017.9:g.35074635_35074637delinsGCA NCBI36
NG_008892.1:g.4511_4513delinsGCA , LRG_210:g.4511_4513delinsGCA
NG_042278.1:g.1876_1878delinsGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-504_-502delinsGCA ENSP00000312624.2:n.-504_-502delinsGCA
Search 100 bp 5'
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