Canonical Allele Identifier: CA400363156
Gene: MTMR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58506839T>C , CM000679.2:g.58506839T>C GRCh38
NC_000017.10:g.56584200T>C , CM000679.1:g.56584200T>C GRCh37
NC_000017.9:g.53939199T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682306.1:c.937A>G MANE Select ENSP00000507664.1:p.Ser313Gly
ENST00000323456.9:c.895A>G ENSP00000325285.5:p.Ser299Gly
ENST00000579925.5:c.895A>G ENSP00000464067.1:p.Ser299Gly
NM_004687.4:c.895A>G NP_004678.3:p.Ser299Gly
XM_005257784.2:c.937A>G XP_005257841.1:p.Ser313Gly
XM_005257785.3:c.907A>G XP_005257842.1:p.Ser303Gly
XM_005257786.3:c.895A>G XP_005257843.1:p.Ser299Gly
XM_006722168.2:c.895A>G XP_006722231.1:p.Ser299Gly
XM_011525460.1:c.907A>G XP_011523762.1:p.Ser303Gly
XM_005257785.5:c.907A>G XP_005257842.1:p.Ser303Gly
XM_005257786.5:c.895A>G XP_005257843.1:p.Ser299Gly
XM_006722168.4:c.895A>G XP_006722231.1:p.Ser299Gly
XM_011525460.3:c.907A>G XP_011523762.1:p.Ser303Gly
NM_004687.5:c.895A>G NP_004678.3:p.Ser299Gly
NM_001378066.1:c.907A>G NP_001364995.1:p.Ser303Gly
NM_001378067.1:c.937A>G MANE Select NP_001364996.1:p.Ser313Gly