Canonical Allele Identifier: CA2478943995

Gene: MTMR11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930294T= , CM000663.2:g.149930294T=	GRCh38
NC_000001.10:g.149902186T= , CM000663.1:g.149902186T=	GRCh37
NC_000001.9:g.148168810T=	NCBI36
NG_032777.1:g.2959A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1647+71A= MANE Select	ENSP00000391668.2:n.1647+71A=
ENST00000369140.7:c.1431+71A=	ENSP00000358136.3:n.1431+71A=
ENST00000439741.2:c.1647+71A=	ENSP00000391668.2:n.1647+71A=
ENST00000466496.5:n.967+71A=
ENST00000482025.5:n.1873+71A=
ENST00000482343.5:n.1471+71A=
ENST00000490310.1:n.850A=
ENST00000492824.5:n.2067+71A=
ENST00000495054.1:n.690+71A=
NM_001145862.1:c.1647+71A=	NP_001139334.1:n.1647+71A=
NM_181873.3:c.1431+71A=	NP_870988.2:n.1431+71A=
XM_006711135.1:c.1539+71A=	XP_006711198.1:n.1539+71A=
XM_006711136.2:c.1431+71A=	XP_006711199.1:n.1431+71A=
XM_006711137.1:c.1431+71A=	XP_006711200.1:n.1431+71A=
XM_011509098.1:c.1563+71A=	XP_011507400.1:n.1563+71A=
XM_011509099.1:c.*676A=	XP_011507401.1:n.*676A=
XR_426759.2:n.1838+71A=
XR_426760.2:n.1744+71A=
XM_011509099.3:c.*676A=	XP_011507401.1:n.*676A=
XM_024452577.1:c.1563+71A=	XP_024308345.1:n.1563+71A=
XM_024452578.1:c.1539+71A=	XP_024308346.1:n.1539+71A=
XR_002959043.1:n.1860+71A=
XR_002959062.1:n.1976+71A=
XR_002959066.1:n.1678+71A=
XR_002959067.1:n.3197+71A=
XR_426760.4:n.1766+71A=
NM_001145862.2:c.1647+71A= MANE Select	NP_001139334.1:n.1647+71A=