Canonical Allele Identifier: CA2647759251

Gene: MTMR11

Linked Data

• gnomAD v4: 1-149930362-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930362C>T , CM000663.2:g.149930362C>T	GRCh38
NC_000001.10:g.149902254C>T , CM000663.1:g.149902254C>T	GRCh37
NC_000001.9:g.148168878C>T	NCBI36
NG_032777.1:g.2891G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1647+3G>A MANE Select	ENSP00000391668.2:n.1647+3G>A
ENST00000369140.7:c.1431+3G>A	ENSP00000358136.3:n.1431+3G>A
ENST00000439741.2:c.1647+3G>A	ENSP00000391668.2:n.1647+3G>A
ENST00000466496.5:n.967+3G>A
ENST00000482025.5:n.1873+3G>A
ENST00000482343.5:n.1471+3G>A
ENST00000490310.1:n.782G>A
ENST00000492824.5:n.2067+3G>A
ENST00000495054.1:n.690+3G>A
NM_001145862.1:c.1647+3G>A	NP_001139334.1:n.1647+3G>A
NM_181873.3:c.1431+3G>A	NP_870988.2:n.1431+3G>A
XM_006711135.1:c.1539+3G>A	XP_006711198.1:n.1539+3G>A
XM_006711136.2:c.1431+3G>A	XP_006711199.1:n.1431+3G>A
XM_006711137.1:c.1431+3G>A	XP_006711200.1:n.1431+3G>A
XM_011509098.1:c.1563+3G>A	XP_011507400.1:n.1563+3G>A
XM_011509099.1:c.*608G>A	XP_011507401.1:n.*608G>A
XR_426759.2:n.1838+3G>A
XR_426760.2:n.1744+3G>A
XM_011509099.3:c.*608G>A	XP_011507401.1:n.*608G>A
XM_024452577.1:c.1563+3G>A	XP_024308345.1:n.1563+3G>A
XM_024452578.1:c.1539+3G>A	XP_024308346.1:n.1539+3G>A
XR_002959043.1:n.1860+3G>A
XR_002959062.1:n.1976+3G>A
XR_002959066.1:n.1678+3G>A
XR_002959067.1:n.3197+3G>A
XR_426760.4:n.1766+3G>A
NM_001145862.2:c.1647+3G>A MANE Select	NP_001139334.1:n.1647+3G>A