Canonical Allele Identifier: CA2478944020

Gene: MTMR11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930377G= , CM000663.2:g.149930377G=	GRCh38
NC_000001.10:g.149902269G= , CM000663.1:g.149902269G=	GRCh37
NC_000001.9:g.148168893G=	NCBI36
NG_032777.1:g.2876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439741.4:c.1635C= MANE Select	ENSP00000391668.2:p.Leu545=
ENST00000369140.7:c.1419C=	ENSP00000358136.3:p.Leu473=
ENST00000439741.2:c.1635C=	ENSP00000391668.2:p.Leu545=
ENST00000466496.5:n.955C=
ENST00000482025.5:n.1861C=
ENST00000482343.5:n.1459C=
ENST00000490310.1:n.767C=
ENST00000492824.5:n.2055C=
ENST00000495054.1:n.678C=
NM_001145862.1:c.1635C=	NP_001139334.1:p.Leu545=
NM_181873.3:c.1419C=	NP_870988.2:p.Leu473=
XM_006711135.1:c.1527C=	XP_006711198.1:p.Leu509=
XM_006711136.2:c.1419C=	XP_006711199.1:p.Leu473=
XM_006711137.1:c.1419C=	XP_006711200.1:p.Leu473=
XM_011509098.1:c.1551C=	XP_011507400.1:p.Leu517=
XM_011509099.1:c.*593C=	XP_011507401.1:n.*593C=
XR_426759.2:n.1826C=
XR_426760.2:n.1732C=
XM_011509099.3:c.*593C=	XP_011507401.1:n.*593C=
XM_024452577.1:c.1551C=	XP_024308345.1:p.Leu517=
XM_024452578.1:c.1527C=	XP_024308346.1:p.Leu509=
XR_002959043.1:n.1848C=
XR_002959062.1:n.1964C=
XR_002959066.1:n.1666C=
XR_002959067.1:n.3185C=
XR_426760.4:n.1754C=
NM_001145862.2:c.1635C= MANE Select	NP_001139334.1:p.Leu545=