Canonical Allele Identifier: CA386637445
Community Standard Title: NM_052845.4(MMAB):c.460G>T (p.Glu154Ter)
Gene: MMAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109561479C>A , CM000674.2:g.109561479C>A GRCh38
NC_000012.11:g.109999284C>A , CM000674.1:g.109999284C>A GRCh37
NC_000012.10:g.108483667C>A NCBI36
NG_007096.1:g.17019G>T

Transcript Alleles

HGVS Amino-acid Change
NM_052845.4:c.460G>T MANE Select NP_443077.1:p.Glu154Ter
ENST00000545712.7:c.460G>T MANE Select ENSP00000445920.1:p.Glu154Ter
NM_052845.3:c.460G>T NP_443077.1:p.Glu154Ter
NR_038118.1:n.533G>T
NR_038118.2:n.484G>T
ENST00000537496.5:c.460G>T ENSP00000444793.1:p.Glu154Ter
ENST00000540016.5:c.304G>T ENSP00000474582.1:p.Glu102Ter
ENST00000541763.6:c.460G>T ENSP00000474981.1:p.Glu154Ter
ENST00000544051.5:c.*254G>T ENSP00000438079.1:n.*254G>T
ENST00000545712.6:c.460G>T ENSP00000445920.1:p.Glu154Ter
XM_011538266.1:c.218G>T XP_011536568.1:p.Gly73Val
XM_011538267.1:c.218G>T XP_011536569.1:p.Gly73Val
XM_011538267.3:c.218G>T XP_011536569.1:p.Gly73Val
XM_011538268.1:c.187G>T XP_011536570.1:p.Glu63Ter
XM_011538268.2:c.187G>T XP_011536570.1:p.Glu63Ter
XM_011538269.1:c.184G>T XP_011536571.1:p.Glu62Ter
XM_011538269.2:c.184G>T XP_011536571.1:p.Glu62Ter
XM_024448961.1:c.460G>T XP_024304729.1:p.Glu154Ter