Canonical Allele Identifier: CA337319604
Gene: MPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154785832C>T , CM000685.2:g.154785832C>T GRCh38
NC_000023.10:g.154014107C>T , CM000685.1:g.154014107C>T GRCh37
NC_000023.9:g.153667301C>T NCBI36
NG_015873.1:g.24696G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369534.8:c.677+372G>A MANE Select ENSP00000358547.3:n.677+372G>A
ENST00000369534.7:c.677+372G>A ENSP00000358547.3:n.677+372G>A
ENST00000393529.5:c.539+372G>A ENSP00000377163.1:n.539+372G>A
ENST00000393531.5:c.617+372G>A ENSP00000377165.1:n.617+372G>A
ENST00000413259.7:c.587+372G>A ENSP00000400155.3:n.587+372G>A
ENST00000428488.1:c.368+372G>A ENSP00000391701.1:n.368+372G>A
ENST00000439370.5:c.*601+372G>A ENSP00000400700.1:n.*601+372G>A
ENST00000453245.5:c.299+372G>A ENSP00000410888.1:n.299+372G>A
ENST00000462825.5:n.268+372G>A
ENST00000475943.5:n.403+372G>A
ENST00000488754.5:n.479+372G>A
ENST00000493871.1:n.22+372G>A
ENST00000494170.1:n.171-2325G>A
NM_001166460.1:c.626+372G>A NP_001159932.1:n.626+372G>A
NM_001166461.1:c.617+372G>A NP_001159933.1:n.617+372G>A
NM_001166462.1:c.587+372G>A NP_001159934.1:n.587+372G>A
NM_002436.3:c.677+372G>A NP_002427.1:n.677+372G>A
XM_011531167.1:c.677+372G>A XP_011529469.1:n.677+372G>A
XM_011531168.1:c.539+372G>A XP_011529470.1:n.539+372G>A
XM_011531169.1:c.299+372G>A XP_011529471.1:n.299+372G>A
XM_011531167.2:c.677+372G>A XP_011529469.1:n.677+372G>A
XM_024452385.1:c.299+372G>A XP_024308153.1:n.299+372G>A
NM_002436.4:c.677+372G>A MANE Select NP_002427.1:n.677+372G>A
NM_001166460.2:c.626+372G>A NP_001159932.1:n.626+372G>A
NM_001166461.2:c.617+372G>A NP_001159933.1:n.617+372G>A
NM_001166462.2:c.587+372G>A NP_001159934.1:n.587+372G>A
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