Canonical Allele Identifier: CA2319604840
Gene: TICAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4816373_4816391delinsCGGGTGAGGCCGTAGGGAA , CM000681.2:g.4816373_4816391delinsCGGGTGAGGCCGTAGGGAA GRCh38
NC_000019.9:g.4816385_4816403delinsCGGGTGAGGCCGTAGGGAA , CM000681.1:g.4816385_4816403delinsCGGGTGAGGCCGTAGGGAA GRCh37
NC_000019.8:g.4767385_4767403delinsCGGGTGAGGCCGTAGGGAA NCBI36
NG_031998.1:g.20352_20370delinsTTCCCTACGGCCTCACCCG , LRG_358:g.20352_20370delinsTTCCCTACGGCCTCACCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000248244.6:c.1987_2005delinsTTCCCTACGGCCTCACCCG MANE Select ENSP00000248244.4:p.Phe663=
ENST00000248244.5:c.1987_2005delinsTTCCCTACGGCCTCACCCG ENSP00000248244.4:p.Phe663=
ENST00000621756.1:c.1489_1507delinsTTCCCTACGGCCTCACCCG ENSP00000479467.1:p.Phe497=
NM_182919.3:c.1987_2005delinsTTCCCTACGGCCTCACCCG , LRG_358t1:c.1987_2005delinsTTCCCTACGGCCTCACCCG NP_891549.1:p.Phe663=
NM_001385678.1:c.1945_1963delinsTTCCCTACGGCCTCACCCG NP_001372607.1:p.Phe649=
NM_001385679.1:c.1852_1870delinsTTCCCTACGGCCTCACCCG NP_001372608.1:p.Phe618=
NM_001385680.1:c.1345_1363delinsTTCCCTACGGCCTCACCCG NP_001372609.1:p.Phe449=
NM_182919.4:c.1987_2005delinsTTCCCTACGGCCTCACCCG MANE Select NP_891549.1:p.Phe663=