Canonical Allele Identifier: CA290865070

Gene: MPP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43887832C>G , CM000679.2:g.43887832C>G	GRCh38
NC_000017.10:g.41965200C>G , CM000679.1:g.41965200C>G	GRCh37
NC_000017.9:g.39320726C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269095.9:c.151-4477G>C MANE Select	ENSP00000269095.4:n.151-4477G>C
ENST00000269095.8:c.151-4477G>C	ENSP00000269095.4:n.151-4477G>C
ENST00000377184.7:c.202-4477G>C	ENSP00000366389.3:n.202-4477G>C
ENST00000461854.5:c.151-3677G>C	ENSP00000428286.1:n.151-3677G>C
ENST00000473246.5:c.118-4477G>C	ENSP00000479767.1:n.118-4477G>C
ENST00000518766.5:c.286-4477G>C	ENSP00000428182.1:n.286-4477G>C
ENST00000520241.5:c.169-4477G>C	ENSP00000428938.1:n.169-4477G>C
ENST00000520305.5:c.-267-4477G>C	ENSP00000428136.1:n.-267-4477G>C
ENST00000520319.1:n.281-4477G>C
ENST00000520406.5:c.151-4477G>C	ENSP00000428354.1:n.151-4477G>C
ENST00000521178.5:c.151-4477G>C	ENSP00000430443.1:n.151-4477G>C
ENST00000522172.5:c.151-4477G>C	ENSP00000430349.1:n.151-4477G>C
ENST00000523220.5:c.100-4477G>C	ENSP00000428468.1:n.100-4477G>C
ENST00000523501.5:c.118-4477G>C	ENSP00000430540.1:n.118-4477G>C
ENST00000523762.5:c.118-4477G>C	ENSP00000428218.1:n.118-4477G>C
ENST00000523934.5:c.151-4477G>C	ENSP00000430797.1:n.151-4477G>C
ENST00000524294.5:c.151-4477G>C	ENSP00000483278.1:n.151-4477G>C
ENST00000536246.5:c.118-4477G>C	ENSP00000438012.1:n.118-4477G>C
ENST00000612133.4:c.151-4477G>C	ENSP00000478528.1:n.151-4477G>C
ENST00000622681.4:c.118-4477G>C	ENSP00000480071.1:n.118-4477G>C
ENST00000625880.2:c.186-4446G>C	ENSP00000486553.1:n.186-4446G>C
NM_001278370.1:c.286-4477G>C	NP_001265299.1:n.286-4477G>C
NM_001278371.1:c.118-4477G>C	NP_001265300.1:n.118-4477G>C
NM_001278372.1:c.151-3677G>C	NP_001265301.1:n.151-3677G>C
NM_001278373.1:c.118-4477G>C	NP_001265302.1:n.118-4477G>C
NM_001278374.1:c.-267-4477G>C	NP_001265303.1:n.-267-4477G>C
NM_001278375.1:c.118-4477G>C	NP_001265304.1:n.118-4477G>C
NM_001278376.2:c.202-4477G>C	NP_001265305.2:n.202-4477G>C
NM_001278381.1:c.151-4477G>C	NP_001265310.1:n.151-4477G>C
NM_005374.4:c.151-4477G>C	NP_005365.4:n.151-4477G>C
XM_011524825.1:c.151-4477G>C	XP_011523127.1:n.151-4477G>C
XM_011524827.1:c.151-3677G>C	XP_011523129.1:n.151-3677G>C
XM_011524827.2:c.313-3677G>C	XP_011523129.2:n.313-3677G>C
XM_024450760.1:c.313-4477G>C	XP_024306528.1:n.313-4477G>C
XM_024450761.1:c.151-4477G>C	XP_024306529.1:n.151-4477G>C
XM_024450762.1:c.151-4477G>C	XP_024306530.1:n.151-4477G>C
XM_024450763.1:c.151-4477G>C	XP_024306531.1:n.151-4477G>C
XR_001752510.2:n.278-4477G>C
XR_001752511.2:n.406-4477G>C
XR_002958008.1:n.378-4477G>C
NM_001278372.2:c.151-3677G>C	NP_001265301.1:n.151-3677G>C
NM_001278373.2:c.118-4477G>C	NP_001265302.1:n.118-4477G>C
NM_001278374.2:c.-267-4477G>C	NP_001265303.1:n.-267-4477G>C
NM_001278376.3:c.202-4477G>C	NP_001265305.2:n.202-4477G>C
NM_005374.5:c.151-4477G>C MANE Select	NP_005365.4:n.151-4477G>C
NM_001278370.2:c.286-4477G>C	NP_001265299.1:n.286-4477G>C
NM_001278371.2:c.118-4477G>C	NP_001265300.1:n.118-4477G>C
NM_001278375.2:c.118-4477G>C	NP_001265304.1:n.118-4477G>C
NM_001278381.2:c.151-4477G>C	NP_001265310.1:n.151-4477G>C