Canonical Allele Identifier: CA2647759175

Gene: MTMR11

Linked Data

• gnomAD v4: 1-149930269-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930271dup , CM000663.2:g.149930271dup	GRCh38
NC_000001.10:g.149902163dup , CM000663.1:g.149902163dup	GRCh37
NC_000001.9:g.148168787dup	NCBI36
NG_032777.1:g.2983dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1647+95dup MANE Select	ENSP00000391668.2:n.1647+95dup
ENST00000369140.7:c.1431+95dup	ENSP00000358136.3:n.1431+95dup
ENST00000439741.2:c.1647+95dup	ENSP00000391668.2:n.1647+95dup
ENST00000466496.5:n.967+95dup
ENST00000482025.5:n.1873+95dup
ENST00000482343.5:n.1471+95dup
ENST00000490310.1:n.874dup
ENST00000492824.5:n.2067+95dup
ENST00000495054.1:n.690+95dup
NM_001145862.1:c.1647+95dup	NP_001139334.1:n.1647+95dup
NM_181873.3:c.1431+95dup	NP_870988.2:n.1431+95dup
XM_006711135.1:c.1539+95dup	XP_006711198.1:n.1539+95dup
XM_006711136.2:c.1431+95dup	XP_006711199.1:n.1431+95dup
XM_006711137.1:c.1431+95dup	XP_006711200.1:n.1431+95dup
XM_011509098.1:c.1563+95dup	XP_011507400.1:n.1563+95dup
XM_011509099.1:c.*700dup	XP_011507401.1:n.*700dup
XR_426759.2:n.1838+95dup
XR_426760.2:n.1744+95dup
XM_011509099.3:c.*700dup	XP_011507401.1:n.*700dup
XM_024452577.1:c.1563+95dup	XP_024308345.1:n.1563+95dup
XM_024452578.1:c.1539+95dup	XP_024308346.1:n.1539+95dup
XR_002959043.1:n.1860+95dup
XR_002959062.1:n.1976+95dup
XR_002959066.1:n.1678+95dup
XR_002959067.1:n.3197+95dup
XR_426760.4:n.1766+95dup
NM_001145862.2:c.1647+95dup MANE Select	NP_001139334.1:n.1647+95dup