Canonical Allele Identifier: CA2062444491

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557393_109557394delinsAC , CM000674.2:g.109557393_109557394delinsAC	GRCh38
NC_000012.11:g.109995198_109995199delinsAC , CM000674.1:g.109995198_109995199delinsAC	GRCh37
NC_000012.10:g.108479581_108479582delinsAC	NCBI36
NG_007096.1:g.21104_21105delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-258_645-257delinsGT MANE Select	ENSP00000445920.1:n.645-258_645-257delinsGT
ENST00000537496.5:c.*210-258_*210-257delinsGT	ENSP00000444793.1:n.*210-258_*210-257delinsGT
ENST00000540016.5:c.489-258_489-257delinsGT	ENSP00000474582.1:n.489-258_489-257delinsGT
ENST00000541763.6:c.870-258_870-257delinsGT	ENSP00000474981.1:n.870-258_870-257delinsGT
ENST00000544051.5:c.*526-258_*526-257delinsGT	ENSP00000438079.1:n.*526-258_*526-257delinsGT
ENST00000545712.6:c.645-258_645-257delinsGT	ENSP00000445920.1:n.645-258_645-257delinsGT
NM_052845.3:c.645-258_645-257delinsGT	NP_443077.1:n.645-258_645-257delinsGT
NR_038118.1:n.805-258_805-257delinsGT
XM_011538266.1:c.490-258_490-257delinsGT	XP_011536568.1:n.490-258_490-257delinsGT
XM_011538267.1:c.490-258_490-257delinsGT	XP_011536569.1:n.490-258_490-257delinsGT
XM_011538268.1:c.372-258_372-257delinsGT	XP_011536570.1:n.372-258_372-257delinsGT
XM_011538269.1:c.369-258_369-257delinsGT	XP_011536571.1:n.369-258_369-257delinsGT
XM_011538267.3:c.490-258_490-257delinsGT	XP_011536569.1:n.490-258_490-257delinsGT
XM_011538268.2:c.372-258_372-257delinsGT	XP_011536570.1:n.372-258_372-257delinsGT
XM_011538269.2:c.369-258_369-257delinsGT	XP_011536571.1:n.369-258_369-257delinsGT
NM_052845.4:c.645-258_645-257delinsGT MANE Select	NP_443077.1:n.645-258_645-257delinsGT
NR_038118.2:n.756-258_756-257delinsGT