Canonical Allele Identifier: CA377782578

Gene: MINPP1

Linked Data

• MyVariant Identifiers: chr10:g.89268174A>T (hg19) ; chr10:g.87508417A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508417A>T , CM000672.2:g.87508417A>T	GRCh38
NC_000010.10:g.89268174A>T , CM000672.1:g.89268174A>T	GRCh37
NC_000010.9:g.89258154A>T	NCBI36
NG_013023.1:g.8952A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.719A>T MANE Select	ENSP00000361064.4:p.Glu240Val
ENST00000371994.8:c.719A>T	ENSP00000361062.4:p.Glu240Val
ENST00000371996.8:c.719A>T	ENSP00000361064.4:p.Glu240Val
ENST00000536010.1:c.116A>T	ENSP00000437823.1:p.Glu39Val
NM_001178117.1:c.719A>T	NP_001171588.1:p.Glu240Val
NM_001178118.1:c.116A>T	NP_001171589.1:p.Glu39Val
NM_004897.4:c.719A>T	NP_004888.2:p.Glu240Val
XM_006718078.2:c.719A>T	XP_006718141.1:p.Glu240Val
XM_011540379.1:c.116A>T	XP_011538681.1:p.Glu39Val
XR_945884.1:n.2843A>T
XM_006718078.3:c.719A>T	XP_006718141.1:p.Glu240Val
XM_011540379.3:c.116A>T	XP_011538681.1:p.Glu39Val
XM_017016965.2:c.719A>T	XP_016872454.1:p.Glu240Val
NM_004897.5:c.719A>T MANE Select	NP_004888.2:p.Glu240Val
NM_001178117.2:c.719A>T	NP_001171588.1:p.Glu240Val
NM_001178118.2:c.116A>T	NP_001171589.1:p.Glu39Val