Canonical Allele Identifier: CA342284317

Gene: MTMR11

Linked Data

• MyVariant Identifiers: chr1:g.149902259G>T (hg19) ; chr1:g.149930367G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930367G>T , CM000663.2:g.149930367G>T	GRCh38
NC_000001.10:g.149902259G>T , CM000663.1:g.149902259G>T	GRCh37
NC_000001.9:g.148168883G>T	NCBI36
NG_032777.1:g.2886C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1645C>A MANE Select	ENSP00000391668.2:p.Gln549Lys
ENST00000369140.7:c.1429C>A	ENSP00000358136.3:p.Gln477Lys
ENST00000439741.2:c.1645C>A	ENSP00000391668.2:p.Gln549Lys
ENST00000466496.5:n.965C>A
ENST00000482025.5:n.1871C>A
ENST00000482343.5:n.1469C>A
ENST00000490310.1:n.777C>A
ENST00000492824.5:n.2065C>A
ENST00000495054.1:n.688C>A
NM_001145862.1:c.1645C>A	NP_001139334.1:p.Gln549Lys
NM_181873.3:c.1429C>A	NP_870988.2:p.Gln477Lys
XM_006711135.1:c.1537C>A	XP_006711198.1:p.Gln513Lys
XM_006711136.2:c.1429C>A	XP_006711199.1:p.Gln477Lys
XM_006711137.1:c.1429C>A	XP_006711200.1:p.Gln477Lys
XM_011509098.1:c.1561C>A	XP_011507400.1:p.Gln521Lys
XM_011509099.1:c.*603C>A	XP_011507401.1:n.*603C>A
XR_426759.2:n.1836C>A
XR_426760.2:n.1742C>A
XM_011509099.3:c.*603C>A	XP_011507401.1:n.*603C>A
XM_024452577.1:c.1561C>A	XP_024308345.1:p.Gln521Lys
XM_024452578.1:c.1537C>A	XP_024308346.1:p.Gln513Lys
XR_002959043.1:n.1858C>A
XR_002959062.1:n.1974C>A
XR_002959066.1:n.1676C>A
XR_002959067.1:n.3195C>A
XR_426760.4:n.1764C>A
NM_001145862.2:c.1645C>A MANE Select	NP_001139334.1:p.Gln549Lys