Canonical Allele Identifier: CA1610189559
Gene: GCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874147_10874153delinsTGGCCCG , CM000668.2:g.10874147_10874153delinsTGGCCCG GRCh38
NC_000006.11:g.10874380_10874386delinsTGGCCCG , CM000668.1:g.10874380_10874386delinsTGGCCCG GRCh37
NC_000006.10:g.10982366_10982372delinsTGGCCCG NCBI36
NG_008970.1:g.12713_12719delinsCGGGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1363_1369delinsCGGGCCA MANE Select ENSP00000368805.4:p.Arg455=
ENST00000379491.4:c.1363_1369delinsCGGGCCA ENSP00000368805.4:p.Arg455=
ENST00000480294.1:c.101-17366_101-17360delinsTGGCCCG ENSP00000417929.1:n.101-17366_101-17360delinsTGGCCCG
NM_004752.3:c.1363_1369delinsCGGGCCA NP_004743.1:p.Arg455=
XM_011514991.1:c.1363_1369delinsCGGGCCA XP_011513293.1:p.Arg455=
NM_004752.4:c.1363_1369delinsCGGGCCA MANE Select NP_004743.1:p.Arg455=