Canonical Allele Identifier: CA2758998311

Gene: MME

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.155118605G>A , CM000665.2:g.155118605G>A	GRCh38
NC_000003.11:g.154836394G>A , CM000665.1:g.154836394G>A	GRCh37
NC_000003.10:g.156319088G>A	NCBI36
NG_051105.1:g.99482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360490.7:c.655-141G>A MANE Select	ENSP00000353679.2:n.655-141G>A
ENST00000460393.6:c.655-141G>A	ENSP00000418525.1:n.655-141G>A
ENST00000473730.6:c.655-141G>A	ENSP00000420542.2:n.655-141G>A
ENST00000491026.6:c.655-141G>A	ENSP00000418791.2:n.655-141G>A
ENST00000615825.2:c.655-141G>A	ENSP00000478173.2:n.655-141G>A
ENST00000675418.2:c.655-141G>A	ENSP00000502021.2:n.655-141G>A
ENST00000679362.1:n.498-141G>A
ENST00000680057.1:c.655-141G>A	ENSP00000505211.1:n.655-141G>A
ENST00000680282.1:c.655-141G>A	ENSP00000505690.1:n.655-141G>A
ENST00000360490.6:c.655-141G>A	ENSP00000353679.2:n.655-141G>A
ENST00000460393.5:c.655-141G>A	ENSP00000418525.1:n.655-141G>A
ENST00000462745.5:c.655-141G>A	ENSP00000419653.1:n.655-141G>A
ENST00000481828.5:c.655-141G>A	ENSP00000420101.1:n.655-141G>A
ENST00000492661.5:c.655-141G>A	ENSP00000420389.1:n.655-141G>A
ENST00000493237.5:c.655-141G>A	ENSP00000417079.1:n.655-141G>A
ENST00000615825.1:c.655-141G>A	ENSP00000478173.1:n.655-141G>A
NM_000902.3:c.655-141G>A	NP_000893.2:n.655-141G>A
NM_007287.2:c.655-141G>A	NP_009218.2:n.655-141G>A
NM_007288.2:c.655-141G>A	NP_009219.2:n.655-141G>A
NM_007289.2:c.655-141G>A	NP_009220.2:n.655-141G>A
XM_006713646.2:c.655-141G>A	XP_006713709.1:n.655-141G>A
XM_006713647.2:c.655-141G>A	XP_006713710.1:n.655-141G>A
XM_011512855.1:c.655-141G>A	XP_011511157.1:n.655-141G>A
XM_011512856.1:c.655-141G>A	XP_011511158.1:n.655-141G>A
XM_011512857.1:c.655-141G>A	XP_011511159.1:n.655-141G>A
XM_011512858.1:c.655-141G>A	XP_011511160.1:n.655-141G>A
NM_001354642.1:c.655-141G>A	NP_001341571.1:n.655-141G>A
NM_001354643.1:c.655-141G>A	NP_001341572.1:n.655-141G>A
NM_007288.3:c.655-141G>A	NP_009219.2:n.655-141G>A
NM_007289.3:c.655-141G>A	NP_009220.2:n.655-141G>A
XM_006713647.4:c.655-141G>A	XP_006713710.1:n.655-141G>A
XM_011512856.2:c.655-141G>A	XP_011511158.1:n.655-141G>A
XM_011512857.2:c.655-141G>A	XP_011511159.1:n.655-141G>A
NM_000902.4:c.655-141G>A	NP_000893.2:n.655-141G>A
NM_007287.3:c.655-141G>A	NP_009218.2:n.655-141G>A
NM_007289.4:c.655-141G>A MANE Select	NP_009220.2:n.655-141G>A
NM_000902.5:c.655-141G>A	NP_000893.2:n.655-141G>A
NM_001354642.2:c.655-141G>A	NP_001341571.1:n.655-141G>A
NM_007287.4:c.655-141G>A	NP_009218.2:n.655-141G>A