Canonical Allele Identifier: CA2638995916

Gene: MTMR4

Linked Data

• gnomAD v4: 17-58506657-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506657C>A , CM000679.2:g.58506657C>A	GRCh38
NC_000017.10:g.56584018C>A , CM000679.1:g.56584018C>A	GRCh37
NC_000017.9:g.53939017C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.1033+86G>T MANE Select	ENSP00000507664.1:n.1033+86G>T
ENST00000323456.9:c.991+86G>T	ENSP00000325285.5:n.991+86G>T
ENST00000579925.5:c.991+86G>T	ENSP00000464067.1:n.991+86G>T
NM_004687.4:c.991+86G>T	NP_004678.3:n.991+86G>T
XM_005257784.2:c.1033+86G>T	XP_005257841.1:n.1033+86G>T
XM_005257785.3:c.1003+86G>T	XP_005257842.1:n.1003+86G>T
XM_005257786.3:c.991+86G>T	XP_005257843.1:n.991+86G>T
XM_006722168.2:c.991+86G>T	XP_006722231.1:n.991+86G>T
XM_011525460.1:c.1003+86G>T	XP_011523762.1:n.1003+86G>T
XM_005257785.5:c.1003+86G>T	XP_005257842.1:n.1003+86G>T
XM_005257786.5:c.991+86G>T	XP_005257843.1:n.991+86G>T
XM_006722168.4:c.991+86G>T	XP_006722231.1:n.991+86G>T
XM_011525460.3:c.1003+86G>T	XP_011523762.1:n.1003+86G>T
NM_004687.5:c.991+86G>T	NP_004678.3:n.991+86G>T
NM_001378066.1:c.1003+86G>T	NP_001364995.1:n.1003+86G>T
NM_001378067.1:c.1033+86G>T MANE Select	NP_001364996.1:n.1033+86G>T