Canonical Allele Identifier: CA2994416108

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557003dup , CM000674.2:g.109557003dup	GRCh38
NC_000012.11:g.109994808dup , CM000674.1:g.109994808dup	GRCh37
NC_000012.10:g.108479191dup	NCBI36
NG_007096.1:g.21496dup

Transcript Alleles

HGVS	Amino-acid Change
NM_052845.4:c.*26dup MANE Select	NP_443077.1:n.*26dup
ENST00000545712.7:c.*26dup MANE Select	ENSP00000445920.1:n.*26dup
NM_052845.3:c.*26dup	NP_443077.1:n.*26dup
NR_038118.1:n.939dup
NR_038118.2:n.890dup
ENST00000537496.5:c.*344dup	ENSP00000444793.1:n.*344dup
ENST00000540016.5:c.*26dup	ENSP00000474582.1:n.*26dup
ENST00000541763.6:c.1004dup	ENSP00000474981.1:n.1004dup
ENST00000544051.5:c.*660dup	ENSP00000438079.1:n.*660dup
ENST00000545712.6:c.*26dup	ENSP00000445920.1:n.*26dup
XM_011538266.1:c.*126dup	XP_011536568.1:n.*126dup
XM_011538267.1:c.*126dup	XP_011536569.1:n.*126dup
XM_011538267.3:c.*126dup	XP_011536569.1:n.*126dup
XM_011538268.1:c.*26dup	XP_011536570.1:n.*26dup
XM_011538268.2:c.*26dup	XP_011536570.1:n.*26dup
XM_011538269.1:c.*26dup	XP_011536571.1:n.*26dup
XM_011538269.2:c.*26dup	XP_011536571.1:n.*26dup