Canonical Allele Identifier: CA307754269
Community Standard Title: NM_002361.4(MAG):c.603_604delinsAA (p.Leu202Met)
Gene: MAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35299741_35299742delinsAA , CM000681.2:g.35299741_35299742delinsAA GRCh38
NC_000019.9:g.35790644_35790645delinsAA , CM000681.1:g.35790644_35790645delinsAA GRCh37
NC_000019.8:g.40482484_40482485delinsAA NCBI36
NG_034078.1:g.12656_12657delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_002361.4:c.603_604delinsAA MANE Select NP_002352.1:p.Leu202Met
ENST00000392213.8:c.603_604delinsAA MANE Select ENSP00000376048.2:p.Leu202Met
NM_001199216.1:c.528_529delinsAA NP_001186145.1:p.Leu177Met
NM_001199216.2:c.528_529delinsAA NP_001186145.1:p.Leu177Met
NM_002361.3:c.603_604delinsAA NP_002352.1:p.Leu202Met
NM_080600.2:c.603_604delinsAA NP_542167.1:p.Leu202Met
NM_080600.3:c.603_604delinsAA NP_542167.1:p.Leu202Met
ENST00000361922.8:c.603_604delinsAA ENSP00000355234.4:p.Leu202Met
ENST00000392213.7:c.603_604delinsAA ENSP00000376048.2:p.Leu202Met
ENST00000537831.2:c.528_529delinsAA ENSP00000440695.1:p.Leu177Met
ENST00000597035.5:c.*187_*188delinsAA ENSP00000473245.1:n.*187_*188delinsAA