Canonical Allele Identifier: CA2315278227
Gene: MBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.76988928G= , CM000680.2:g.76988928G= GRCh38
NC_000018.9:g.74700884G= , CM000680.1:g.74700884G= GRCh37
NC_000018.8:g.72829872G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355994.7:c.682-16C= MANE Select ENSP00000348273.2:n.682-16C=
ENST00000354542.4:c.178-8457C= ENSP00000346545.4:n.178-8457C=
ENST00000355994.6:c.682-16C= ENSP00000348273.2:n.682-16C=
ENST00000359645.7:c.361-16C= ENSP00000352667.3:n.361-16C=
ENST00000382582.7:c.361-16C= ENSP00000372025.3:n.361-16C=
ENST00000397865.9:c.283-16C= ENSP00000380963.5:n.283-16C=
ENST00000397866.8:c.283-16C= ENSP00000380964.4:n.283-16C=
ENST00000397868.6:n.330-16C=
ENST00000397869.7:c.283-16C= ENSP00000380967.3:n.283-16C=
ENST00000397875.7:c.297C= ENSP00000380973.3:p.Phe99=
ENST00000447114.5:c.115-16C= ENSP00000405882.1:n.115-16C=
ENST00000459948.1:c.*71C= ENSP00000435322.1:n.*71C=
ENST00000467108.1:n.333-16C=
ENST00000473302.5:c.*43C= ENSP00000432988.1:n.*43C=
ENST00000483025.5:c.*170-16C= ENSP00000442393.1:n.*170-16C=
ENST00000484548.6:n.317-16C=
ENST00000493623.5:c.*81C= ENSP00000436951.1:n.*81C=
ENST00000526111.5:c.217-16C= ENSP00000435641.1:n.217-16C=
ENST00000527041.1:c.227+1083C= ENSP00000435243.1:n.227+1083C=
ENST00000527975.5:c.*32-16C= ENSP00000431267.1:n.*32-16C=
ENST00000528160.1:c.96-4127C= ENSP00000436830.1:n.96-4127C=
ENST00000531144.5:c.*21-16C= ENSP00000431335.1:n.*21-16C=
ENST00000533278.5:c.*21-16C= ENSP00000434011.1:n.*21-16C=
ENST00000577755.5:c.170-408C=
ENST00000578193.5:c.283-16C= ENSP00000463403.1:n.283-16C=
ENST00000578873.5:c.361-16C= ENSP00000463137.1:n.361-16C=
ENST00000579129.5:c.682-16C= ENSP00000463780.1:n.682-16C=
ENST00000580402.5:c.682-16C= ENSP00000462223.1:n.682-16C=
ENST00000580473.5:n.431-16C=
ENST00000581179.5:n.408-16C=
ENST00000582282.5:n.326-16C=
ENST00000583118.5:n.158-16C=
ENST00000583474.5:c.*21-16C= ENSP00000462758.1:n.*21-16C=
ENST00000585201.5:c.69-16C=
ENST00000585216.5:n.330-16C=
NM_001025081.1:c.361-16C= NP_001020252.1:n.361-16C=
NM_001025090.1:c.283-16C= NP_001020261.1:n.283-16C=
NM_001025092.1:c.283-16C= NP_001020263.1:n.283-16C=
NM_001025101.1:c.682-16C= NP_001020272.1:n.682-16C=
NM_002385.2:c.361-16C= NP_002376.1:n.361-16C=
XM_011526008.1:c.682-16C= XP_011524310.1:n.682-16C=
XM_011526009.1:c.682-16C= XP_011524311.1:n.682-16C=
XM_011526010.1:c.682-16C= XP_011524312.1:n.682-16C=
XM_011526011.1:c.682-16C= XP_011524313.1:n.682-16C=
XR_245460.2:n.941-16C=
XR_245461.2:n.941-16C=
XM_024451185.1:c.760-16C= XP_024306953.1:n.760-16C=
XM_024451186.1:c.760-16C= XP_024306954.1:n.760-16C=
XM_024451187.1:c.760-16C= XP_024306955.1:n.760-16C=
XM_024451188.1:c.361-16C= XP_024306956.1:n.361-16C=
XR_001753201.1:n.614-16C=
XR_001753202.1:n.614-16C=
NM_001025101.2:c.682-16C= MANE Select NP_001020272.1:n.682-16C=
NM_001025081.2:c.361-16C= NP_001020252.1:n.361-16C=
NM_001025090.2:c.283-16C= NP_001020261.1:n.283-16C=
NM_001025092.2:c.283-16C= NP_001020263.1:n.283-16C=
NM_002385.3:c.361-16C= NP_002376.1:n.361-16C=