Canonical Allele Identifier: CA2187901531

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896026C= , CM000677.2:g.74896026C=	GRCh38
NC_000015.9:g.75188367C= , CM000677.1:g.75188367C=	GRCh37
NC_000015.8:g.72975420C=	NCBI36
NG_008921.1:g.10958C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.671-126C= MANE Select	ENSP00000318318.6:n.671-126C=
ENST00000323744.10:c.488-126C=	ENSP00000318192.6:n.488-126C=
ENST00000352410.8:c.671-126C=	ENSP00000318318.6:n.671-126C=
ENST00000535694.5:c.521-126C=	ENSP00000440447.1:n.521-126C=
ENST00000561470.5:c.*567-126C=	ENSP00000454267.1:n.*567-126C=
ENST00000562606.5:c.611-126C=	ENSP00000457020.1:n.611-126C=
ENST00000562800.5:c.256-1513C=	ENSP00000457619.1:n.256-1513C=
ENST00000563422.5:c.671-126C=	ENSP00000457885.1:n.671-126C=
ENST00000563786.5:c.611-126C=	ENSP00000455241.1:n.611-126C=
ENST00000564003.5:c.338-126C=	ENSP00000454312.1:n.338-126C=
ENST00000566377.5:c.671-126C=	ENSP00000455405.1:n.671-126C=
ENST00000566556.1:n.593C=
ENST00000567177.1:c.449-126C=	ENSP00000457013.1:n.449-126C=
ENST00000569931.5:c.611-126C=	ENSP00000455161.1:n.611-126C=
NM_001289155.1:c.671-126C=	NP_001276084.1:n.671-126C=
NM_001289156.1:c.521-126C=	NP_001276085.1:n.521-126C=
NM_001289157.1:c.488-126C=	NP_001276086.1:n.488-126C=
NM_002435.2:c.671-126C=	NP_002426.1:n.671-126C=
XM_011521592.1:c.659-126C=	XP_011519894.1:n.659-126C=
XM_011521593.1:c.611-126C=	XP_011519895.1:n.611-126C=
NM_001330372.1:c.611-126C=	NP_001317301.1:n.611-126C=
XM_017022208.1:c.611-126C=	XP_016877697.1:n.611-126C=
XM_017022209.2:c.521-126C=	XP_016877698.1:n.521-126C=
NM_002435.3:c.671-126C= MANE Select	NP_002426.1:n.671-126C=
NM_001289155.2:c.671-126C=	NP_001276084.1:n.671-126C=
NM_001289156.2:c.521-126C=	NP_001276085.1:n.521-126C=
NM_001289157.2:c.488-126C=	NP_001276086.1:n.488-126C=
NM_001330372.2:c.611-126C=	NP_001317301.1:n.611-126C=