Canonical Allele Identifier: CA2478944015

Gene: MTMR11

Linked Data

• dbSNP Id: rs2092641874
• gnomAD v3: 1-149930361-T-G
• gnomAD v4: 1-149930361-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930361T>G , CM000663.2:g.149930361T>G	GRCh38
NC_000001.10:g.149902253T>G , CM000663.1:g.149902253T>G	GRCh37
NC_000001.9:g.148168877T>G	NCBI36
NG_032777.1:g.2892A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1647+4A>C MANE Select	ENSP00000391668.2:n.1647+4A>C
ENST00000369140.7:c.1431+4A>C	ENSP00000358136.3:n.1431+4A>C
ENST00000439741.2:c.1647+4A>C	ENSP00000391668.2:n.1647+4A>C
ENST00000466496.5:n.967+4A>C
ENST00000482025.5:n.1873+4A>C
ENST00000482343.5:n.1471+4A>C
ENST00000490310.1:n.783A>C
ENST00000492824.5:n.2067+4A>C
ENST00000495054.1:n.690+4A>C
NM_001145862.1:c.1647+4A>C	NP_001139334.1:n.1647+4A>C
NM_181873.3:c.1431+4A>C	NP_870988.2:n.1431+4A>C
XM_006711135.1:c.1539+4A>C	XP_006711198.1:n.1539+4A>C
XM_006711136.2:c.1431+4A>C	XP_006711199.1:n.1431+4A>C
XM_006711137.1:c.1431+4A>C	XP_006711200.1:n.1431+4A>C
XM_011509098.1:c.1563+4A>C	XP_011507400.1:n.1563+4A>C
XM_011509099.1:c.*609A>C	XP_011507401.1:n.*609A>C
XR_426759.2:n.1838+4A>C
XR_426760.2:n.1744+4A>C
XM_011509099.3:c.*609A>C	XP_011507401.1:n.*609A>C
XM_024452577.1:c.1563+4A>C	XP_024308345.1:n.1563+4A>C
XM_024452578.1:c.1539+4A>C	XP_024308346.1:n.1539+4A>C
XR_002959043.1:n.1860+4A>C
XR_002959062.1:n.1976+4A>C
XR_002959066.1:n.1678+4A>C
XR_002959067.1:n.3197+4A>C
XR_426760.4:n.1766+4A>C
NM_001145862.2:c.1647+4A>C MANE Select	NP_001139334.1:n.1647+4A>C