Canonical Allele Identifier: CA501060506

Gene: MTMR4

Linked Data

• MyVariant Identifiers: chr17:g.56584204C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506843C>G , CM000679.2:g.58506843C>G	GRCh38
NC_000017.10:g.56584204C>G , CM000679.1:g.56584204C>G	GRCh37
NC_000017.9:g.53939203C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.933G>C MANE Select	ENSP00000507664.1:p.Val311=
ENST00000323456.9:c.891G>C	ENSP00000325285.5:p.Val297=
ENST00000579925.5:c.891G>C	ENSP00000464067.1:p.Val297=
NM_004687.4:c.891G>C	NP_004678.3:p.Val297=
XM_005257784.2:c.933G>C	XP_005257841.1:p.Val311=
XM_005257785.3:c.903G>C	XP_005257842.1:p.Val301=
XM_005257786.3:c.891G>C	XP_005257843.1:p.Val297=
XM_006722168.2:c.891G>C	XP_006722231.1:p.Val297=
XM_011525460.1:c.903G>C	XP_011523762.1:p.Val301=
XM_005257785.5:c.903G>C	XP_005257842.1:p.Val301=
XM_005257786.5:c.891G>C	XP_005257843.1:p.Val297=
XM_006722168.4:c.891G>C	XP_006722231.1:p.Val297=
XM_011525460.3:c.903G>C	XP_011523762.1:p.Val301=
NM_004687.5:c.891G>C	NP_004678.3:p.Val297=
NM_001378066.1:c.903G>C	NP_001364995.1:p.Val301=
NM_001378067.1:c.933G>C MANE Select	NP_001364996.1:p.Val311=