Canonical Allele Identifier: CA2647759172

Gene: MTMR11

Linked Data

• gnomAD v4: 1-149930267-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930267C>A , CM000663.2:g.149930267C>A	GRCh38
NC_000001.10:g.149902159C>A , CM000663.1:g.149902159C>A	GRCh37
NC_000001.9:g.148168783C>A	NCBI36
NG_032777.1:g.2986G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1647+98G>T MANE Select	ENSP00000391668.2:n.1647+98G>T
ENST00000369140.7:c.1431+98G>T	ENSP00000358136.3:n.1431+98G>T
ENST00000439741.2:c.1647+98G>T	ENSP00000391668.2:n.1647+98G>T
ENST00000466496.5:n.967+98G>T
ENST00000482025.5:n.1873+98G>T
ENST00000482343.5:n.1471+98G>T
ENST00000490310.1:n.877G>T
ENST00000492824.5:n.2067+98G>T
ENST00000495054.1:n.690+98G>T
NM_001145862.1:c.1647+98G>T	NP_001139334.1:n.1647+98G>T
NM_181873.3:c.1431+98G>T	NP_870988.2:n.1431+98G>T
XM_006711135.1:c.1539+98G>T	XP_006711198.1:n.1539+98G>T
XM_006711136.2:c.1431+98G>T	XP_006711199.1:n.1431+98G>T
XM_006711137.1:c.1431+98G>T	XP_006711200.1:n.1431+98G>T
XM_011509098.1:c.1563+98G>T	XP_011507400.1:n.1563+98G>T
XM_011509099.1:c.*703G>T	XP_011507401.1:n.*703G>T
XR_426759.2:n.1838+98G>T
XR_426760.2:n.1744+98G>T
XM_011509099.3:c.*703G>T	XP_011507401.1:n.*703G>T
XM_024452577.1:c.1563+98G>T	XP_024308345.1:n.1563+98G>T
XM_024452578.1:c.1539+98G>T	XP_024308346.1:n.1539+98G>T
XR_002959043.1:n.1860+98G>T
XR_002959062.1:n.1976+98G>T
XR_002959066.1:n.1678+98G>T
XR_002959067.1:n.3197+98G>T
XR_426760.4:n.1766+98G>T
NM_001145862.2:c.1647+98G>T MANE Select	NP_001139334.1:n.1647+98G>T