Canonical Allele Identifier: CA2677312254
Gene: GCM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874247_10874248insGG , CM000668.2:g.10874247_10874248insGG GRCh38
NC_000006.11:g.10874480_10874481insGG , CM000668.1:g.10874480_10874481insGG GRCh37
NC_000006.10:g.10982466_10982467insGG NCBI36
NG_008970.1:g.12618_12619insCC

Transcript Alleles

HGVS Amino-acid change
ENST00000379491.5:c.1268_1269insCC MANE Select ENSP00000368805.4:p.Met423IlefsTer13
ENST00000379491.4:c.1268_1269insCC ENSP00000368805.4:p.Met423IlefsTer13
ENST00000480294.1:c.101-17266_101-17265insGG ENSP00000417929.1:n.101-17266_101-17265in...
NM_004752.3:c.1268_1269insCC NP_004743.1:p.Met423IlefsTer13
XM_011514991.1:c.1268_1269insCC XP_011513293.1:p.Met423IlefsTer13
NM_004752.4:c.1268_1269insCC MANE Select NP_004743.1:p.Met423IlefsTer13