Canonical Allele Identifier: CA2576334508
Gene: MTMR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58506660C>G , CM000679.2:g.58506660C>G GRCh38
NC_000017.10:g.56584021C>G , CM000679.1:g.56584021C>G GRCh37
NC_000017.9:g.53939020C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682306.1:c.1033+83G>C MANE Select ENSP00000507664.1:n.1033+83G>C
ENST00000323456.9:c.991+83G>C ENSP00000325285.5:n.991+83G>C
ENST00000579925.5:c.991+83G>C ENSP00000464067.1:n.991+83G>C
NM_004687.4:c.991+83G>C NP_004678.3:n.991+83G>C
XM_005257784.2:c.1033+83G>C XP_005257841.1:n.1033+83G>C
XM_005257785.3:c.1003+83G>C XP_005257842.1:n.1003+83G>C
XM_005257786.3:c.991+83G>C XP_005257843.1:n.991+83G>C
XM_006722168.2:c.991+83G>C XP_006722231.1:n.991+83G>C
XM_011525460.1:c.1003+83G>C XP_011523762.1:n.1003+83G>C
XM_005257785.5:c.1003+83G>C XP_005257842.1:n.1003+83G>C
XM_005257786.5:c.991+83G>C XP_005257843.1:n.991+83G>C
XM_006722168.4:c.991+83G>C XP_006722231.1:n.991+83G>C
XM_011525460.3:c.1003+83G>C XP_011523762.1:n.1003+83G>C
NM_004687.5:c.991+83G>C NP_004678.3:n.991+83G>C
NM_001378066.1:c.1003+83G>C NP_001364995.1:n.1003+83G>C
NM_001378067.1:c.1033+83G>C MANE Select NP_001364996.1:n.1033+83G>C