Canonical Allele Identifier: CA2575285610

Gene: MMAB

Linked Data

• gnomAD v4: 12-109568918-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568919del , CM000674.2:g.109568919del	GRCh38
NC_000012.11:g.110006724del , CM000674.1:g.110006724del	GRCh37
NC_000012.10:g.108491107del	NCBI36
NG_007096.1:g.9579del
NG_007702.1:g.225del , LRG_156:g.225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.197-56del MANE Select	ENSP00000445920.1:n.197-56del
ENST00000420167.6:c.*26-56del	ENSP00000416136.2:n.*26-56del
ENST00000503497.7:c.197-56del	ENSP00000474881.1:n.197-56del
ENST00000536760.1:n.200-56del
ENST00000537236.2:c.197-56del	ENSP00000483818.1:n.197-56del
ENST00000537496.5:c.197-56del	ENSP00000444793.1:n.197-56del
ENST00000540016.5:c.135-3743del	ENSP00000474582.1:n.135-3743del
ENST00000541763.6:c.197-56del	ENSP00000474981.1:n.197-56del
ENST00000542390.5:n.224-56del
ENST00000544051.5:c.135-56del	ENSP00000438079.1:n.135-56del
ENST00000545712.6:c.197-56del	ENSP00000445920.1:n.197-56del
NM_052845.3:c.197-56del	NP_443077.1:n.197-56del
NR_038118.1:n.270-56del
XM_024448961.1:c.197-56del	XP_024304729.1:n.197-56del
NM_052845.4:c.197-56del MANE Select	NP_443077.1:n.197-56del
NR_038118.2:n.221-56del