Canonical Allele Identifier: CA1610190123
Gene: GCM2 HGNC NCBI

Linked Data

dbSNP Id: rs1779845257

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10874357_10874358insTGT , CM000668.2:g.10874357_10874358insTGT GRCh38
NC_000006.11:g.10874590_10874591insTGT , CM000668.1:g.10874590_10874591insTGT GRCh37
NC_000006.10:g.10982576_10982577insTGT NCBI36
NG_008970.1:g.12510_12511insAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000379491.5:c.1160_1161insAAC MANE Select ENSP00000368805.4:p.Thr387_Lys388insThr
ENST00000379491.4:c.1160_1161insAAC ENSP00000368805.4:p.Thr387_Lys388insThr
ENST00000480294.1:c.101-17156_101-17155insTGT ENSP00000417929.1:n.101-17156_101-17155insTGT
NM_004752.3:c.1160_1161insAAC NP_004743.1:p.Thr387_Lys388insThr
XM_011514991.1:c.1160_1161insAAC XP_011513293.1:p.Thr387_Lys388insThr
NM_004752.4:c.1160_1161insAAC MANE Select NP_004743.1:p.Thr387_Lys388insThr