Canonical Allele Identifier: CA2797414379
Gene: MMAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109560971_109560972insCCCCCCCCCCCCCCCCCCCCCCCCTCCGTCCTCCTCTCCCTC , CM000674.2:g.109560971_109560972insCCCCCCCCCCCCCCCCCCCCCCCCTCCGTCCTCCTCTCCCTC GRCh38
NC_000012.11:g.109998776_109998777insCCCCCCCCCCCCCCCCCCCCCCCCTCCGTCCTCCTCTCCCTC , CM000674.1:g.109998776_109998777insCCCCCCCCCCCCCCCCCCCCCCCCTCCGTCCTCCTCTCCCTC GRCh37
NC_000012.10:g.108483159_108483160insCCCCCCCCCCCCCCCCCCCCCCCCTCCGTCCTCCTCTCCCTC NCBI36
NG_007096.1:g.17545_17546insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000545712.7:c.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG MANE Select ENSP00000445920.1:n.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGA...
ENST00000537496.5:c.*149+87_*149+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG ENSP00000444793.1:n.*149+87_*149+88insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000540016.5:c.428+87_428+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG ENSP00000474582.1:n.428+87_428+88insGGGGGGGGGGGGGGGGGGGGGGGGA...
ENST00000541763.6:c.809+87_809+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG ENSP00000474981.1:n.809+87_809+88insGGGGGGGGGGGGGGGGGGGGGGGGA...
ENST00000544051.5:c.*465+87_*465+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG ENSP00000438079.1:n.*465+87_*465+88insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000545712.6:c.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG ENSP00000445920.1:n.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGA...
NM_052845.3:c.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG NP_443077.1:n.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGA...
NR_038118.1:n.744+87_744+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG
XM_011538266.1:c.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536568.1:n.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538267.1:c.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536569.1:n.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538268.1:c.311+87_311+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536570.1:n.311+87_311+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538269.1:c.308+87_308+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536571.1:n.308+87_308+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538267.3:c.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536569.1:n.429+87_429+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538268.2:c.311+87_311+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536570.1:n.311+87_311+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_011538269.2:c.308+87_308+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_011536571.1:n.308+87_308+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
XM_024448961.1:c.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG XP_024304729.1:n.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGG...
NM_052845.4:c.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG MANE Select NP_443077.1:n.584+87_584+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGA...
NR_038118.2:n.695+87_695+88insGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGAGGACGGAG