Canonical Allele Identifier: CA2620808922

Gene: MMAB

Linked Data

• gnomAD v4: 12-109560941-CCCTCTCCCCATCTCCGTCCTCCTCTCCCTCTCCCTCCCCCCTCCCCCTTGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109560950_109561001del , CM000674.2:g.109560950_109561001del	GRCh38
NC_000012.11:g.109998755_109998806del , CM000674.1:g.109998755_109998806del	GRCh37
NC_000012.10:g.108483138_108483189del	NCBI36
NG_007096.1:g.17505_17556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.584+47_584+98del MANE Select	ENSP00000445920.1:n.584+47_584+98del
ENST00000537496.5:c.*149+47_*149+98del	ENSP00000444793.1:n.*149+47_*149+98del
ENST00000540016.5:c.428+47_428+98del	ENSP00000474582.1:n.428+47_428+98del
ENST00000541763.6:c.809+47_809+98del	ENSP00000474981.1:n.809+47_809+98del
ENST00000544051.5:c.*465+47_*465+98del	ENSP00000438079.1:n.*465+47_*465+98del
ENST00000545712.6:c.584+47_584+98del	ENSP00000445920.1:n.584+47_584+98del
NM_052845.3:c.584+47_584+98del	NP_443077.1:n.584+47_584+98del
NR_038118.1:n.744+47_744+98del
XM_011538266.1:c.429+47_429+98del	XP_011536568.1:n.429+47_429+98del
XM_011538267.1:c.429+47_429+98del	XP_011536569.1:n.429+47_429+98del
XM_011538268.1:c.311+47_311+98del	XP_011536570.1:n.311+47_311+98del
XM_011538269.1:c.308+47_308+98del	XP_011536571.1:n.308+47_308+98del
XM_011538267.3:c.429+47_429+98del	XP_011536569.1:n.429+47_429+98del
XM_011538268.2:c.311+47_311+98del	XP_011536570.1:n.311+47_311+98del
XM_011538269.2:c.308+47_308+98del	XP_011536571.1:n.308+47_308+98del
XM_024448961.1:c.584+47_584+98del	XP_024304729.1:n.584+47_584+98del
NM_052845.4:c.584+47_584+98del MANE Select	NP_443077.1:n.584+47_584+98del
NR_038118.2:n.695+47_695+98del