Canonical Allele Identifier: CA2620809804

Gene: MMAB

Linked Data

• gnomAD v4: 12-109560976-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109560976_109560977insAG , CM000674.2:g.109560976_109560977insAG	GRCh38
NC_000012.11:g.109998781_109998782insAG , CM000674.1:g.109998781_109998782insAG	GRCh37
NC_000012.10:g.108483164_108483165insAG	NCBI36
NG_007096.1:g.17521_17522insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.584+63_584+64insCT MANE Select	ENSP00000445920.1:n.584+63_584+64insCT
ENST00000537496.5:c.*149+63_*149+64insCT	ENSP00000444793.1:n.*149+63_*149+64insCT
ENST00000540016.5:c.428+63_428+64insCT	ENSP00000474582.1:n.428+63_428+64insCT
ENST00000541763.6:c.809+63_809+64insCT	ENSP00000474981.1:n.809+63_809+64insCT
ENST00000544051.5:c.*465+63_*465+64insCT	ENSP00000438079.1:n.*465+63_*465+64insCT
ENST00000545712.6:c.584+63_584+64insCT	ENSP00000445920.1:n.584+63_584+64insCT
NM_052845.3:c.584+63_584+64insCT	NP_443077.1:n.584+63_584+64insCT
NR_038118.1:n.744+63_744+64insCT
XM_011538266.1:c.429+63_429+64insCT	XP_011536568.1:n.429+63_429+64insCT
XM_011538267.1:c.429+63_429+64insCT	XP_011536569.1:n.429+63_429+64insCT
XM_011538268.1:c.311+63_311+64insCT	XP_011536570.1:n.311+63_311+64insCT
XM_011538269.1:c.308+63_308+64insCT	XP_011536571.1:n.308+63_308+64insCT
XM_011538267.3:c.429+63_429+64insCT	XP_011536569.1:n.429+63_429+64insCT
XM_011538268.2:c.311+63_311+64insCT	XP_011536570.1:n.311+63_311+64insCT
XM_011538269.2:c.308+63_308+64insCT	XP_011536571.1:n.308+63_308+64insCT
XM_024448961.1:c.584+63_584+64insCT	XP_024304729.1:n.584+63_584+64insCT
NM_052845.4:c.584+63_584+64insCT MANE Select	NP_443077.1:n.584+63_584+64insCT
NR_038118.2:n.695+63_695+64insCT