Canonical Allele Identifier: CA2062444410

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557343_109557344delinsGT , CM000674.2:g.109557343_109557344delinsGT	GRCh38
NC_000012.11:g.109995148_109995149delinsGT , CM000674.1:g.109995148_109995149delinsGT	GRCh37
NC_000012.10:g.108479531_108479532delinsGT	NCBI36
NG_007096.1:g.21154_21155delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-208_645-207delinsAC MANE Select	ENSP00000445920.1:n.645-208_645-207delinsAC
ENST00000537496.5:c.*210-208_*210-207delinsAC	ENSP00000444793.1:n.*210-208_*210-207delinsAC
ENST00000540016.5:c.489-208_489-207delinsAC	ENSP00000474582.1:n.489-208_489-207delinsAC
ENST00000541763.6:c.870-208_870-207delinsAC	ENSP00000474981.1:n.870-208_870-207delinsAC
ENST00000544051.5:c.*526-208_*526-207delinsAC	ENSP00000438079.1:n.*526-208_*526-207delinsAC
ENST00000545712.6:c.645-208_645-207delinsAC	ENSP00000445920.1:n.645-208_645-207delinsAC
NM_052845.3:c.645-208_645-207delinsAC	NP_443077.1:n.645-208_645-207delinsAC
NR_038118.1:n.805-208_805-207delinsAC
XM_011538266.1:c.490-208_490-207delinsAC	XP_011536568.1:n.490-208_490-207delinsAC
XM_011538267.1:c.490-208_490-207delinsAC	XP_011536569.1:n.490-208_490-207delinsAC
XM_011538268.1:c.372-208_372-207delinsAC	XP_011536570.1:n.372-208_372-207delinsAC
XM_011538269.1:c.369-208_369-207delinsAC	XP_011536571.1:n.369-208_369-207delinsAC
XM_011538267.3:c.490-208_490-207delinsAC	XP_011536569.1:n.490-208_490-207delinsAC
XM_011538268.2:c.372-208_372-207delinsAC	XP_011536570.1:n.372-208_372-207delinsAC
XM_011538269.2:c.369-208_369-207delinsAC	XP_011536571.1:n.369-208_369-207delinsAC
NM_052845.4:c.645-208_645-207delinsAC MANE Select	NP_443077.1:n.645-208_645-207delinsAC
NR_038118.2:n.756-208_756-207delinsAC