Canonical Allele Identifier: CA2259200418
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665230_39665233delinsTCCC , CM000679.2:g.39665230_39665233delinsTCCC GRCh38
NC_000017.10:g.37821483_37821486delinsTCCC , CM000679.1:g.37821483_37821486delinsTCCC GRCh37
NC_000017.9:g.35075009_35075012delinsTCCC NCBI36
NG_008892.1:g.4885_4888delinsTCCC , LRG_210:g.4885_4888delinsTCCC
NG_042278.1:g.2250_2253delinsTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-130_-127delinsTCCC ENSP00000312624.2:n.-130_-127delinsTCCC