Canonical Allele Identifier: CA168107079
Gene: MGAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142040800G>C , CM000669.2:g.142040800G>C GRCh38
NC_000007.12:g.141387069G>C NCBI36
NG_033954.1:g.49922G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000475668.6:c.2452G>C MANE Select ENSP00000417515.2:p.Gly818Arg
ENST00000549489.6:c.2452G>C ENSP00000447378.2:p.Gly818Arg
ENST00000620571.1:c.2452G>C ENSP00000482292.1:p.Gly818Arg
NM_004668.2:c.2452G>C NP_004659.2:p.Gly818Arg
XM_006716168.2:c.2452G>C XP_006716231.1:p.Gly818Arg
XM_011516670.1:c.2452G>C XP_011514972.1:p.Gly818Arg
XM_011516671.1:c.2452G>C XP_011514973.1:p.Gly818Arg
XM_011516672.1:c.2452G>C XP_011514974.1:p.Gly818Arg
XM_011516673.1:c.2452G>C XP_011514975.1:p.Gly818Arg
XM_011516674.1:c.2452G>C XP_011514976.1:p.Gly818Arg
XR_927545.1:n.2564G>C
NM_001365693.1:c.2452G>C MANE Select NP_001352622.1:p.Gly818Arg
XM_011516670.2:c.2452G>C XP_011514972.1:p.Gly818Arg
XM_011516671.2:c.2452G>C XP_011514973.1:p.Gly818Arg
XM_011516672.2:c.2452G>C XP_011514974.1:p.Gly818Arg
XM_011516673.2:c.2452G>C XP_011514975.1:p.Gly818Arg
XM_011516674.2:c.2452G>C XP_011514976.1:p.Gly818Arg
XM_017012772.1:c.2452G>C XP_016868261.1:p.Gly818Arg
XM_024446990.1:c.2452G>C XP_024302758.1:p.Gly818Arg
NM_004668.3:c.2452G>C NP_004659.2:p.Gly818Arg