Canonical Allele Identifier: CA342284395

Gene: MTMR11

Linked Data

• MyVariant Identifiers: chr1:g.149902268G>T (hg19) ; chr1:g.149930376G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930376G>T , CM000663.2:g.149930376G>T	GRCh38
NC_000001.10:g.149902268G>T , CM000663.1:g.149902268G>T	GRCh37
NC_000001.9:g.148168892G>T	NCBI36
NG_032777.1:g.2877C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439741.4:c.1636C>A MANE Select	ENSP00000391668.2:p.Pro546Thr
ENST00000369140.7:c.1420C>A	ENSP00000358136.3:p.Pro474Thr
ENST00000439741.2:c.1636C>A	ENSP00000391668.2:p.Pro546Thr
ENST00000466496.5:n.956C>A
ENST00000482025.5:n.1862C>A
ENST00000482343.5:n.1460C>A
ENST00000490310.1:n.768C>A
ENST00000492824.5:n.2056C>A
ENST00000495054.1:n.679C>A
NM_001145862.1:c.1636C>A	NP_001139334.1:p.Pro546Thr
NM_181873.3:c.1420C>A	NP_870988.2:p.Pro474Thr
XM_006711135.1:c.1528C>A	XP_006711198.1:p.Pro510Thr
XM_006711136.2:c.1420C>A	XP_006711199.1:p.Pro474Thr
XM_006711137.1:c.1420C>A	XP_006711200.1:p.Pro474Thr
XM_011509098.1:c.1552C>A	XP_011507400.1:p.Pro518Thr
XM_011509099.1:c.*594C>A	XP_011507401.1:n.*594C>A
XR_426759.2:n.1827C>A
XR_426760.2:n.1733C>A
XM_011509099.3:c.*594C>A	XP_011507401.1:n.*594C>A
XM_024452577.1:c.1552C>A	XP_024308345.1:p.Pro518Thr
XM_024452578.1:c.1528C>A	XP_024308346.1:p.Pro510Thr
XR_002959043.1:n.1849C>A
XR_002959062.1:n.1965C>A
XR_002959066.1:n.1667C>A
XR_002959067.1:n.3186C>A
XR_426760.4:n.1755C>A
NM_001145862.2:c.1636C>A MANE Select	NP_001139334.1:p.Pro546Thr