Canonical Allele Identifier: CA470851377

Gene: MINPP1

Linked Data

• dbSNP Id: rs1230048134
• MyVariant Identifiers: chr10:g.89268169A>G (hg19) ; chr10:g.87508412A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508412A>G , CM000672.2:g.87508412A>G	GRCh38
NC_000010.10:g.89268169A>G , CM000672.1:g.89268169A>G	GRCh37
NC_000010.9:g.89258149A>G	NCBI36
NG_013023.1:g.8947A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.714A>G MANE Select	ENSP00000361064.4:p.Glu238=
ENST00000371994.8:c.714A>G	ENSP00000361062.4:p.Glu238=
ENST00000371996.8:c.714A>G	ENSP00000361064.4:p.Glu238=
ENST00000536010.1:c.111A>G	ENSP00000437823.1:p.Glu37=
NM_001178117.1:c.714A>G	NP_001171588.1:p.Glu238=
NM_001178118.1:c.111A>G	NP_001171589.1:p.Glu37=
NM_004897.4:c.714A>G	NP_004888.2:p.Glu238=
XM_006718078.2:c.714A>G	XP_006718141.1:p.Glu238=
XM_011540379.1:c.111A>G	XP_011538681.1:p.Glu37=
XR_945884.1:n.2838A>G
XM_006718078.3:c.714A>G	XP_006718141.1:p.Glu238=
XM_011540379.3:c.111A>G	XP_011538681.1:p.Glu37=
XM_017016965.2:c.714A>G	XP_016872454.1:p.Glu238=
NM_004897.5:c.714A>G MANE Select	NP_004888.2:p.Glu238=
NM_001178117.2:c.714A>G	NP_001171588.1:p.Glu238=
NM_001178118.2:c.111A>G	NP_001171589.1:p.Glu37=