Canonical Allele Identifier: CA2620810342

Gene: MMAB

Linked Data

• gnomAD v4: 12-109557146-CAGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557154_109557157del , CM000674.2:g.109557154_109557157del	GRCh38
NC_000012.11:g.109994959_109994962del , CM000674.1:g.109994959_109994962del	GRCh37
NC_000012.10:g.108479342_108479345del	NCBI36
NG_007096.1:g.21348_21351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-14_645-11del MANE Select	ENSP00000445920.1:n.645-14_645-11del
ENST00000537496.5:c.*210-14_*210-11del	ENSP00000444793.1:n.*210-14_*210-11del
ENST00000540016.5:c.489-14_489-11del	ENSP00000474582.1:n.489-14_489-11del
ENST00000541763.6:c.870-14_870-11del	ENSP00000474981.1:n.870-14_870-11del
ENST00000544051.5:c.*526-14_*526-11del	ENSP00000438079.1:n.*526-14_*526-11del
ENST00000545712.6:c.645-14_645-11del	ENSP00000445920.1:n.645-14_645-11del
NM_052845.3:c.645-14_645-11del	NP_443077.1:n.645-14_645-11del
NR_038118.1:n.805-14_805-11del
XM_011538266.1:c.490-14_490-11del	XP_011536568.1:n.490-14_490-11del
XM_011538267.1:c.490-14_490-11del	XP_011536569.1:n.490-14_490-11del
XM_011538268.1:c.372-14_372-11del	XP_011536570.1:n.372-14_372-11del
XM_011538269.1:c.369-14_369-11del	XP_011536571.1:n.369-14_369-11del
XM_011538267.3:c.490-14_490-11del	XP_011536569.1:n.490-14_490-11del
XM_011538268.2:c.372-14_372-11del	XP_011536570.1:n.372-14_372-11del
XM_011538269.2:c.369-14_369-11del	XP_011536571.1:n.369-14_369-11del
NM_052845.4:c.645-14_645-11del MANE Select	NP_443077.1:n.645-14_645-11del
NR_038118.2:n.756-14_756-11del