Canonical Allele Identifier: CA342284345

Gene: MTMR11

Linked Data

• MyVariant Identifiers: chr1:g.149902263T>A (hg19) ; chr1:g.149930371T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930371T>A , CM000663.2:g.149930371T>A	GRCh38
NC_000001.10:g.149902263T>A , CM000663.1:g.149902263T>A	GRCh37
NC_000001.9:g.148168887T>A	NCBI36
NG_032777.1:g.2882A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1641A>T MANE Select	ENSP00000391668.2:p.Arg547Ser
ENST00000369140.7:c.1425A>T	ENSP00000358136.3:p.Arg475Ser
ENST00000439741.2:c.1641A>T	ENSP00000391668.2:p.Arg547Ser
ENST00000466496.5:n.961A>T
ENST00000482025.5:n.1867A>T
ENST00000482343.5:n.1465A>T
ENST00000490310.1:n.773A>T
ENST00000492824.5:n.2061A>T
ENST00000495054.1:n.684A>T
NM_001145862.1:c.1641A>T	NP_001139334.1:p.Arg547Ser
NM_181873.3:c.1425A>T	NP_870988.2:p.Arg475Ser
XM_006711135.1:c.1533A>T	XP_006711198.1:p.Arg511Ser
XM_006711136.2:c.1425A>T	XP_006711199.1:p.Arg475Ser
XM_006711137.1:c.1425A>T	XP_006711200.1:p.Arg475Ser
XM_011509098.1:c.1557A>T	XP_011507400.1:p.Arg519Ser
XM_011509099.1:c.*599A>T	XP_011507401.1:n.*599A>T
XR_426759.2:n.1832A>T
XR_426760.2:n.1738A>T
XM_011509099.3:c.*599A>T	XP_011507401.1:n.*599A>T
XM_024452577.1:c.1557A>T	XP_024308345.1:p.Arg519Ser
XM_024452578.1:c.1533A>T	XP_024308346.1:p.Arg511Ser
XR_002959043.1:n.1854A>T
XR_002959062.1:n.1970A>T
XR_002959066.1:n.1672A>T
XR_002959067.1:n.3191A>T
XR_426760.4:n.1760A>T
NM_001145862.2:c.1641A>T MANE Select	NP_001139334.1:p.Arg547Ser