Canonical Allele Identifier: CA342284410

Gene: MTMR11

Linked Data

• MyVariant Identifiers: chr1:g.149902273C>G (hg19) ; chr1:g.149930381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930381C>G , CM000663.2:g.149930381C>G	GRCh38
NC_000001.10:g.149902273C>G , CM000663.1:g.149902273C>G	GRCh37
NC_000001.9:g.148168897C>G	NCBI36
NG_032777.1:g.2872G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000439741.4:c.1631G>C MANE Select	ENSP00000391668.2:p.Trp544Ser
ENST00000369140.7:c.1415G>C	ENSP00000358136.3:p.Trp472Ser
ENST00000439741.2:c.1631G>C	ENSP00000391668.2:p.Trp544Ser
ENST00000466496.5:n.951G>C
ENST00000482025.5:n.1857G>C
ENST00000482343.5:n.1455G>C
ENST00000490310.1:n.763G>C
ENST00000492824.5:n.2051G>C
ENST00000495054.1:n.674G>C
NM_001145862.1:c.1631G>C	NP_001139334.1:p.Trp544Ser
NM_181873.3:c.1415G>C	NP_870988.2:p.Trp472Ser
XM_006711135.1:c.1523G>C	XP_006711198.1:p.Trp508Ser
XM_006711136.2:c.1415G>C	XP_006711199.1:p.Trp472Ser
XM_006711137.1:c.1415G>C	XP_006711200.1:p.Trp472Ser
XM_011509098.1:c.1547G>C	XP_011507400.1:p.Trp516Ser
XM_011509099.1:c.*589G>C	XP_011507401.1:n.*589G>C
XR_426759.2:n.1822G>C
XR_426760.2:n.1728G>C
XM_011509099.3:c.*589G>C	XP_011507401.1:n.*589G>C
XM_024452577.1:c.1547G>C	XP_024308345.1:p.Trp516Ser
XM_024452578.1:c.1523G>C	XP_024308346.1:p.Trp508Ser
XR_002959043.1:n.1844G>C
XR_002959062.1:n.1960G>C
XR_002959066.1:n.1662G>C
XR_002959067.1:n.3181G>C
XR_426760.4:n.1750G>C
NM_001145862.2:c.1631G>C MANE Select	NP_001139334.1:p.Trp544Ser