Canonical Allele Identifier: CA2647759201

Gene: MTMR11

Linked Data

• gnomAD v4: 1-149930295-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930295C>G , CM000663.2:g.149930295C>G	GRCh38
NC_000001.10:g.149902187C>G , CM000663.1:g.149902187C>G	GRCh37
NC_000001.9:g.148168811C>G	NCBI36
NG_032777.1:g.2958G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439741.4:c.1647+70G>C MANE Select	ENSP00000391668.2:n.1647+70G>C
ENST00000369140.7:c.1431+70G>C	ENSP00000358136.3:n.1431+70G>C
ENST00000439741.2:c.1647+70G>C	ENSP00000391668.2:n.1647+70G>C
ENST00000466496.5:n.967+70G>C
ENST00000482025.5:n.1873+70G>C
ENST00000482343.5:n.1471+70G>C
ENST00000490310.1:n.849G>C
ENST00000492824.5:n.2067+70G>C
ENST00000495054.1:n.690+70G>C
NM_001145862.1:c.1647+70G>C	NP_001139334.1:n.1647+70G>C
NM_181873.3:c.1431+70G>C	NP_870988.2:n.1431+70G>C
XM_006711135.1:c.1539+70G>C	XP_006711198.1:n.1539+70G>C
XM_006711136.2:c.1431+70G>C	XP_006711199.1:n.1431+70G>C
XM_006711137.1:c.1431+70G>C	XP_006711200.1:n.1431+70G>C
XM_011509098.1:c.1563+70G>C	XP_011507400.1:n.1563+70G>C
XM_011509099.1:c.*675G>C	XP_011507401.1:n.*675G>C
XR_426759.2:n.1838+70G>C
XR_426760.2:n.1744+70G>C
XM_011509099.3:c.*675G>C	XP_011507401.1:n.*675G>C
XM_024452577.1:c.1563+70G>C	XP_024308345.1:n.1563+70G>C
XM_024452578.1:c.1539+70G>C	XP_024308346.1:n.1539+70G>C
XR_002959043.1:n.1860+70G>C
XR_002959062.1:n.1976+70G>C
XR_002959066.1:n.1678+70G>C
XR_002959067.1:n.3197+70G>C
XR_426760.4:n.1766+70G>C
NM_001145862.2:c.1647+70G>C MANE Select	NP_001139334.1:n.1647+70G>C