Canonical Allele Identifier: CA951704840

Gene: MMAB

Linked Data

• gnomAD v3: 12-109568902-T-A
• gnomAD v4: 12-109568902-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568902T>A , CM000674.2:g.109568902T>A	GRCh38
NC_000012.11:g.110006707T>A , CM000674.1:g.110006707T>A	GRCh37
NC_000012.10:g.108491090T>A	NCBI36
NG_007096.1:g.9596A>T
NG_007702.1:g.208T>A , LRG_156:g.208T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.197-39A>T MANE Select	ENSP00000445920.1:n.197-39A>T
ENST00000420167.6:c.*26-39A>T	ENSP00000416136.2:n.*26-39A>T
ENST00000503497.7:c.197-39A>T	ENSP00000474881.1:n.197-39A>T
ENST00000536760.1:n.200-39A>T
ENST00000537236.2:c.197-39A>T	ENSP00000483818.1:n.197-39A>T
ENST00000537496.5:c.197-39A>T	ENSP00000444793.1:n.197-39A>T
ENST00000540016.5:c.135-3726A>T	ENSP00000474582.1:n.135-3726A>T
ENST00000541763.6:c.197-39A>T	ENSP00000474981.1:n.197-39A>T
ENST00000542390.5:n.224-39A>T
ENST00000544051.5:c.135-39A>T	ENSP00000438079.1:n.135-39A>T
ENST00000545712.6:c.197-39A>T	ENSP00000445920.1:n.197-39A>T
NM_052845.3:c.197-39A>T	NP_443077.1:n.197-39A>T
NR_038118.1:n.270-39A>T
XM_024448961.1:c.197-39A>T	XP_024304729.1:n.197-39A>T
NM_052845.4:c.197-39A>T MANE Select	NP_443077.1:n.197-39A>T
NR_038118.2:n.221-39A>T