Canonical Allele Identifier: CA14600477
Gene: MPPE1 HGNC NCBI

Linked Data

dbSNP Id: rs593713
gnomAD v2: 18-11887657-G-A
gnomAD v3: 18-11887658-G-A
gnomAD v4: 18-11887658-G-A
MyVariant Identifiers: chr18:g.11887657G>A (hg19) chr18:g.11887658G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.11887658G>A , CM000680.2:g.11887658G>A GRCh38
NC_000018.9:g.11887657G>A , CM000680.1:g.11887657G>A GRCh37
NC_000018.8:g.11877657G>A NCBI36
NG_033866.1:g.203644G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588072.6:c.570-633C>T MANE Select ENSP00000465894.1:n.570-633C>T
ENST00000309976.13:c.570-633C>T ENSP00000311200.9:n.570-633C>T
ENST00000317235.11:c.570-633C>T ENSP00000327257.6:n.570-633C>T
ENST00000317251.8:c.279-633C>T ENSP00000312935.4:n.279-633C>T
ENST00000344987.11:c.570-633C>T ENSP00000339423.7:n.570-633C>T
ENST00000496196.5:c.570-633C>T ENSP00000433950.1:n.570-633C>T
ENST00000587724.5:c.30-633C>T ENSP00000466291.1:n.30-633C>T
ENST00000588072.5:c.570-633C>T ENSP00000465894.1:n.570-633C>T
ENST00000589731.5:n.884-633C>T
ENST00000592331.5:c.348-633C>T ENSP00000466303.1:n.348-633C>T
ENST00000592447.5:n.583-633C>T
ENST00000592894.5:n.469-633C>T
ENST00000592977.5:c.570-633C>T ENSP00000468606.1:n.570-633C>T
NM_001242904.1:c.570-633C>T NP_001229833.1:n.570-633C>T
NM_023075.5:c.570-633C>T NP_075563.3:n.570-633C>T
NR_040241.1:n.1366-633C>T
NR_040242.1:n.1234-633C>T
NR_040243.1:n.1366-633C>T
XM_006722340.2:c.570-633C>T XP_006722403.1:n.570-633C>T
XM_006722341.2:c.570-633C>T XP_006722404.1:n.570-633C>T
XM_006722342.2:c.570-633C>T XP_006722405.1:n.570-633C>T
XM_006722343.2:c.570-633C>T XP_006722406.1:n.570-633C>T
XM_006722345.2:c.570-633C>T XP_006722408.1:n.570-633C>T
XM_006722346.1:c.570-633C>T XP_006722409.1:n.570-633C>T
XM_006722347.2:c.570-633C>T XP_006722410.1:n.570-633C>T
XM_006722348.1:c.570-633C>T XP_006722411.1:n.570-633C>T
XM_011525731.1:c.570-633C>T XP_011524033.1:n.570-633C>T
XM_011525732.1:c.570-633C>T XP_011524034.1:n.570-633C>T
XM_011525733.1:c.570-633C>T XP_011524035.1:n.570-633C>T
XM_011525734.1:c.570-633C>T XP_011524036.1:n.570-633C>T
XR_935068.1:n.919-633C>T
NM_001319154.1:c.570-633C>T NP_001306083.1:n.570-633C>T
NM_001330563.1:c.570-633C>T NP_001317492.1:n.570-633C>T
NR_040242.3:n.1234-633C>T
XM_006722340.3:c.570-633C>T XP_006722403.1:n.570-633C>T
XM_006722341.4:c.570-633C>T XP_006722404.1:n.570-633C>T
XM_006722342.4:c.570-633C>T XP_006722405.1:n.570-633C>T
XM_006722343.3:c.570-633C>T XP_006722406.1:n.570-633C>T
XM_006722345.4:c.570-633C>T XP_006722408.1:n.570-633C>T
XM_006722346.3:c.570-633C>T XP_006722409.1:n.570-633C>T
XM_006722348.2:c.570-633C>T XP_006722411.1:n.570-633C>T
XM_011525731.3:c.570-633C>T XP_011524033.1:n.570-633C>T
XM_011525732.2:c.570-633C>T XP_011524034.1:n.570-633C>T
XM_011525734.2:c.570-633C>T XP_011524036.1:n.570-633C>T
XM_017025920.2:c.570-633C>T XP_016881409.1:n.570-633C>T
XM_017025922.2:c.570-633C>T XP_016881411.1:n.570-633C>T
XM_017025923.2:c.570-633C>T XP_016881412.1:n.570-633C>T
XM_017025924.2:c.570-633C>T XP_016881413.1:n.570-633C>T
XM_017025925.1:c.570-633C>T XP_016881414.1:n.570-633C>T
XM_017025926.2:c.570-633C>T XP_016881415.1:n.570-633C>T
XM_017025927.2:c.570-633C>T XP_016881416.1:n.570-633C>T
XM_017025928.1:c.570-633C>T XP_016881417.1:n.570-633C>T
XM_017025929.2:c.570-633C>T XP_016881418.1:n.570-633C>T
XM_017025930.2:c.570-633C>T XP_016881419.1:n.570-633C>T
XM_017025931.1:c.570-633C>T XP_016881420.1:n.570-633C>T
XM_024451237.1:c.570-633C>T XP_024307005.1:n.570-633C>T
XR_001753261.1:n.1446-633C>T
XR_001753262.2:n.1718-633C>T
XR_001753263.2:n.812-633C>T
XR_001753264.2:n.916-633C>T
XR_001753265.2:n.812-633C>T
XR_002958183.1:n.745-633C>T
XR_002958184.1:n.812-633C>T
XR_935068.3:n.916-633C>T
NM_001242904.2:c.570-633C>T NP_001229833.1:n.570-633C>T
NM_001319154.2:c.570-633C>T NP_001306083.1:n.570-633C>T
NM_001330563.2:c.570-633C>T NP_001317492.1:n.570-633C>T
NM_023075.6:c.570-633C>T MANE Select NP_075563.3:n.570-633C>T
NR_040241.2:n.886-633C>T
NR_040242.4:n.754-633C>T
NR_040243.2:n.886-633C>T
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