Canonical Allele Identifier: CA1925983121

Gene: MINPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508463A= , CM000672.2:g.87508463A=	GRCh38
NC_000010.10:g.89268220A= , CM000672.1:g.89268220A=	GRCh37
NC_000010.9:g.89258200A=	NCBI36
NG_013023.1:g.8998A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371996.9:c.765A= MANE Select	ENSP00000361064.4:p.Gly255=
ENST00000371994.8:c.765A=	ENSP00000361062.4:p.Gly255=
ENST00000371996.8:c.765A=	ENSP00000361064.4:p.Gly255=
ENST00000536010.1:c.162A=	ENSP00000437823.1:p.Gly54=
NM_001178117.1:c.765A=	NP_001171588.1:p.Gly255=
NM_001178118.1:c.162A=	NP_001171589.1:p.Gly54=
NM_004897.4:c.765A=	NP_004888.2:p.Gly255=
XM_006718078.2:c.765A=	XP_006718141.1:p.Gly255=
XM_011540379.1:c.162A=	XP_011538681.1:p.Gly54=
XR_945884.1:n.2889A=
XM_006718078.3:c.765A=	XP_006718141.1:p.Gly255=
XM_011540379.3:c.162A=	XP_011538681.1:p.Gly54=
XM_017016965.2:c.765A=	XP_016872454.1:p.Gly255=
NM_004897.5:c.765A= MANE Select	NP_004888.2:p.Gly255=
NM_001178117.2:c.765A=	NP_001171588.1:p.Gly255=
NM_001178118.2:c.162A=	NP_001171589.1:p.Gly54=