Canonical Allele Identifier: CA2245902139
Gene: MPDU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7587859G>A , CM000679.2:g.7587859G>A GRCh38
NC_000017.10:g.7491177G>A , CM000679.1:g.7491177G>A GRCh37
NC_000017.9:g.7431901G>A NCBI36
NG_009204.1:g.9213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000250124.11:c.*308G>A MANE Select ENSP00000250124.6:n.*308G>A
ENST00000250124.10:c.*308G>A ENSP00000250124.6:n.*308G>A
ENST00000396501.8:c.*415G>A ENSP00000379758.4:n.*415G>A
ENST00000423172.6:c.532+588G>A ENSP00000414071.2:n.532+588G>A
ENST00000572836.5:n.1206G>A
ENST00000574558.1:c.821G>A
ENST00000577088.5:n.1327G>A
ENST00000584378.5:c.413+588G>A ENSP00000462839.1:n.413+588G>A
ENST00000585217.5:c.346-236G>A ENSP00000463037.1:n.346-236G>A
ENST00000620608.4:c.*415G>A ENSP00000483915.1:n.*415G>A
ENST00000621041.4:c.*150G>A ENSP00000479257.1:n.*150G>A
NM_004870.3:c.*308G>A NP_004861.2:n.*308G>A
NR_024603.1:n.1263G>A
XM_006721597.1:c.*150G>A XP_006721660.1:n.*150G>A
XM_006721598.1:c.*415G>A XP_006721661.1:n.*415G>A
XM_006721599.1:c.*415G>A XP_006721662.1:n.*415G>A
XM_011524081.1:c.*308G>A XP_011522383.1:n.*308G>A
NM_001330073.1:c.*415G>A NP_001317002.1:n.*415G>A
XM_006721597.2:c.*150G>A XP_006721660.1:n.*150G>A
XM_006721598.3:c.*415G>A XP_006721661.1:n.*415G>A
XM_011524081.2:c.*308G>A XP_011522383.1:n.*308G>A
XM_024451040.1:c.*308G>A XP_024306808.1:n.*308G>A
NM_004870.4:c.*308G>A MANE Select NP_004861.2:n.*308G>A