Canonical Allele Identifier: CA2620810371

Gene: MMAB

Linked Data

• gnomAD v4: 12-109557179-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557184_109557185del , CM000674.2:g.109557184_109557185del	GRCh38
NC_000012.11:g.109994989_109994990del , CM000674.1:g.109994989_109994990del	GRCh37
NC_000012.10:g.108479372_108479373del	NCBI36
NG_007096.1:g.21317_21318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-45_645-44del MANE Select	ENSP00000445920.1:n.645-45_645-44del
ENST00000537496.5:c.*210-45_*210-44del	ENSP00000444793.1:n.*210-45_*210-44del
ENST00000540016.5:c.489-45_489-44del	ENSP00000474582.1:n.489-45_489-44del
ENST00000541763.6:c.870-45_870-44del	ENSP00000474981.1:n.870-45_870-44del
ENST00000544051.5:c.*526-45_*526-44del	ENSP00000438079.1:n.*526-45_*526-44del
ENST00000545712.6:c.645-45_645-44del	ENSP00000445920.1:n.645-45_645-44del
NM_052845.3:c.645-45_645-44del	NP_443077.1:n.645-45_645-44del
NR_038118.1:n.805-45_805-44del
XM_011538266.1:c.490-45_490-44del	XP_011536568.1:n.490-45_490-44del
XM_011538267.1:c.490-45_490-44del	XP_011536569.1:n.490-45_490-44del
XM_011538268.1:c.372-45_372-44del	XP_011536570.1:n.372-45_372-44del
XM_011538269.1:c.369-45_369-44del	XP_011536571.1:n.369-45_369-44del
XM_011538267.3:c.490-45_490-44del	XP_011536569.1:n.490-45_490-44del
XM_011538268.2:c.372-45_372-44del	XP_011536570.1:n.372-45_372-44del
XM_011538269.2:c.369-45_369-44del	XP_011536571.1:n.369-45_369-44del
NM_052845.4:c.645-45_645-44del MANE Select	NP_443077.1:n.645-45_645-44del
NR_038118.2:n.756-45_756-44del