Canonical Allele Identifier: CA1925983122

Gene: MINPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508470A= , CM000672.2:g.87508470A=	GRCh38
NC_000010.10:g.89268227A= , CM000672.1:g.89268227A=	GRCh37
NC_000010.9:g.89258207A=	NCBI36
NG_013023.1:g.9005A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371996.9:c.772A= MANE Select	ENSP00000361064.4:p.Met258=
ENST00000371994.8:c.772A=	ENSP00000361062.4:p.Met258=
ENST00000371996.8:c.772A=	ENSP00000361064.4:p.Met258=
ENST00000536010.1:c.169A=	ENSP00000437823.1:p.Met57=
NM_001178117.1:c.772A=	NP_001171588.1:p.Met258=
NM_001178118.1:c.169A=	NP_001171589.1:p.Met57=
NM_004897.4:c.772A=	NP_004888.2:p.Met258=
XM_006718078.2:c.772A=	XP_006718141.1:p.Met258=
XM_011540379.1:c.169A=	XP_011538681.1:p.Met57=
XR_945884.1:n.2896A=
XM_006718078.3:c.772A=	XP_006718141.1:p.Met258=
XM_011540379.3:c.169A=	XP_011538681.1:p.Met57=
XM_017016965.2:c.772A=	XP_016872454.1:p.Met258=
NM_004897.5:c.772A= MANE Select	NP_004888.2:p.Met258=
NM_001178117.2:c.772A=	NP_001171588.1:p.Met258=
NM_001178118.2:c.169A=	NP_001171589.1:p.Met57=