Canonical Allele Identifier: CA2809978990
Gene: MTMR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58506678dup , CM000679.2:g.58506678dup GRCh38
NC_000017.10:g.56584039dup , CM000679.1:g.56584039dup GRCh37
NC_000017.9:g.53939038dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682306.1:c.1033+66dup MANE Select ENSP00000507664.1:n.1033+66dup
ENST00000323456.9:c.991+66dup ENSP00000325285.5:n.991+66dup
ENST00000579925.5:c.991+66dup ENSP00000464067.1:n.991+66dup
NM_004687.4:c.991+66dup NP_004678.3:n.991+66dup
XM_005257784.2:c.1033+66dup XP_005257841.1:n.1033+66dup
XM_005257785.3:c.1003+66dup XP_005257842.1:n.1003+66dup
XM_005257786.3:c.991+66dup XP_005257843.1:n.991+66dup
XM_006722168.2:c.991+66dup XP_006722231.1:n.991+66dup
XM_011525460.1:c.1003+66dup XP_011523762.1:n.1003+66dup
XM_005257785.5:c.1003+66dup XP_005257842.1:n.1003+66dup
XM_005257786.5:c.991+66dup XP_005257843.1:n.991+66dup
XM_006722168.4:c.991+66dup XP_006722231.1:n.991+66dup
XM_011525460.3:c.1003+66dup XP_011523762.1:n.1003+66dup
NM_004687.5:c.991+66dup NP_004678.3:n.991+66dup
NM_001378066.1:c.1003+66dup NP_001364995.1:n.1003+66dup
NM_001378067.1:c.1033+66dup MANE Select NP_001364996.1:n.1033+66dup