Canonical Allele Identifier: CA2062443942

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109556999G= , CM000674.2:g.109556999G=	GRCh38
NC_000012.11:g.109994804G= , CM000674.1:g.109994804G=	GRCh37
NC_000012.10:g.108479187G=	NCBI36
NG_007096.1:g.21499C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*29C= MANE Select	ENSP00000445920.1:n.*29C=
ENST00000537496.5:c.*347C=	ENSP00000444793.1:n.*347C=
ENST00000540016.5:c.*29C=	ENSP00000474582.1:n.*29C=
ENST00000541763.6:c.1007C=	ENSP00000474981.1:n.1007C=
ENST00000544051.5:c.*663C=	ENSP00000438079.1:n.*663C=
ENST00000545712.6:c.*29C=	ENSP00000445920.1:n.*29C=
NM_052845.3:c.*29C=	NP_443077.1:n.*29C=
NR_038118.1:n.942C=
XM_011538266.1:c.*129C=	XP_011536568.1:n.*129C=
XM_011538267.1:c.*129C=	XP_011536569.1:n.*129C=
XM_011538268.1:c.*29C=	XP_011536570.1:n.*29C=
XM_011538269.1:c.*29C=	XP_011536571.1:n.*29C=
XM_011538267.3:c.*129C=	XP_011536569.1:n.*129C=
XM_011538268.2:c.*29C=	XP_011536570.1:n.*29C=
XM_011538269.2:c.*29C=	XP_011536571.1:n.*29C=
NM_052845.4:c.*29C= MANE Select	NP_443077.1:n.*29C=
NR_038118.2:n.893C=