Canonical Allele Identifier: CA420675640

Gene: MTMR11

Linked Data

• MyVariant Identifiers: chr1:g.149902266A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930374A>G , CM000663.2:g.149930374A>G	GRCh38
NC_000001.10:g.149902266A>G , CM000663.1:g.149902266A>G	GRCh37
NC_000001.9:g.148168890A>G	NCBI36
NG_032777.1:g.2879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439741.4:c.1638T>C MANE Select	ENSP00000391668.2:p.Pro546=
ENST00000369140.7:c.1422T>C	ENSP00000358136.3:p.Pro474=
ENST00000439741.2:c.1638T>C	ENSP00000391668.2:p.Pro546=
ENST00000466496.5:n.958T>C
ENST00000482025.5:n.1864T>C
ENST00000482343.5:n.1462T>C
ENST00000490310.1:n.770T>C
ENST00000492824.5:n.2058T>C
ENST00000495054.1:n.681T>C
NM_001145862.1:c.1638T>C	NP_001139334.1:p.Pro546=
NM_181873.3:c.1422T>C	NP_870988.2:p.Pro474=
XM_006711135.1:c.1530T>C	XP_006711198.1:p.Pro510=
XM_006711136.2:c.1422T>C	XP_006711199.1:p.Pro474=
XM_006711137.1:c.1422T>C	XP_006711200.1:p.Pro474=
XM_011509098.1:c.1554T>C	XP_011507400.1:p.Pro518=
XM_011509099.1:c.*596T>C	XP_011507401.1:n.*596T>C
XR_426759.2:n.1829T>C
XR_426760.2:n.1735T>C
XM_011509099.3:c.*596T>C	XP_011507401.1:n.*596T>C
XM_024452577.1:c.1554T>C	XP_024308345.1:p.Pro518=
XM_024452578.1:c.1530T>C	XP_024308346.1:p.Pro510=
XR_002959043.1:n.1851T>C
XR_002959062.1:n.1967T>C
XR_002959066.1:n.1669T>C
XR_002959067.1:n.3188T>C
XR_426760.4:n.1757T>C
NM_001145862.2:c.1638T>C MANE Select	NP_001139334.1:p.Pro546=