Canonical Allele Identifier: CA1925981592

Gene: MINPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87505037C= , CM000672.2:g.87505037C=	GRCh38
NC_000010.10:g.89264794C= , CM000672.1:g.89264794C=	GRCh37
NC_000010.9:g.89254774C=	NCBI36
NG_013023.1:g.5572C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004897.5:c.122C= MANE Select	NP_004888.2:p.Ser41=
ENST00000371996.9:c.122C= MANE Select	ENSP00000361064.4:p.Ser41=
NM_001178117.1:c.122C=	NP_001171588.1:p.Ser41=
NM_001178117.2:c.122C=	NP_001171588.1:p.Ser41=
NM_004897.4:c.122C=	NP_004888.2:p.Ser41=
ENST00000371994.8:c.122C=	ENSP00000361062.4:p.Ser41=
ENST00000371996.8:c.122C=	ENSP00000361064.4:p.Ser41=
XM_006718078.2:c.122C=	XP_006718141.1:p.Ser41=
XM_006718078.3:c.122C=	XP_006718141.1:p.Ser41=
XM_011540379.3:c.-592C=	XP_011538681.1:n.-592C=
XM_017016965.2:c.122C=	XP_016872454.1:p.Ser41=
XR_945884.1:n.2246C=