Canonical Allele Identifier: CA501060369

Gene: MTMR4

Linked Data

• MyVariant Identifiers: chr17:g.56584120T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506759T>G , CM000679.2:g.58506759T>G	GRCh38
NC_000017.10:g.56584120T>G , CM000679.1:g.56584120T>G	GRCh37
NC_000017.9:g.53939119T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.1017A>C MANE Select	ENSP00000507664.1:p.Gly339=
ENST00000323456.9:c.975A>C	ENSP00000325285.5:p.Gly325=
ENST00000579925.5:c.975A>C	ENSP00000464067.1:p.Gly325=
NM_004687.4:c.975A>C	NP_004678.3:p.Gly325=
XM_005257784.2:c.1017A>C	XP_005257841.1:p.Gly339=
XM_005257785.3:c.987A>C	XP_005257842.1:p.Gly329=
XM_005257786.3:c.975A>C	XP_005257843.1:p.Gly325=
XM_006722168.2:c.975A>C	XP_006722231.1:p.Gly325=
XM_011525460.1:c.987A>C	XP_011523762.1:p.Gly329=
XM_005257785.5:c.987A>C	XP_005257842.1:p.Gly329=
XM_005257786.5:c.975A>C	XP_005257843.1:p.Gly325=
XM_006722168.4:c.975A>C	XP_006722231.1:p.Gly325=
XM_011525460.3:c.987A>C	XP_011523762.1:p.Gly329=
NM_004687.5:c.975A>C	NP_004678.3:p.Gly325=
NM_001378066.1:c.987A>C	NP_001364995.1:p.Gly329=
NM_001378067.1:c.1017A>C MANE Select	NP_001364996.1:p.Gly339=