Canonical Allele Identifier: CA2062443901

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109556972C= , CM000674.2:g.109556972C=	GRCh38
NC_000012.11:g.109994777C= , CM000674.1:g.109994777C=	GRCh37
NC_000012.10:g.108479160C=	NCBI36
NG_007096.1:g.21526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*56G= MANE Select	ENSP00000445920.1:n.*56G=
ENST00000537496.5:c.*374G=	ENSP00000444793.1:n.*374G=
ENST00000540016.5:c.*56G=	ENSP00000474582.1:n.*56G=
ENST00000541763.6:c.1034G=	ENSP00000474981.1:n.1034G=
ENST00000544051.5:c.*690G=	ENSP00000438079.1:n.*690G=
ENST00000545712.6:c.*56G=	ENSP00000445920.1:n.*56G=
NM_052845.3:c.*56G=	NP_443077.1:n.*56G=
NR_038118.1:n.969G=
XM_011538266.1:c.*156G=	XP_011536568.1:n.*156G=
XM_011538267.1:c.*156G=	XP_011536569.1:n.*156G=
XM_011538268.1:c.*56G=	XP_011536570.1:n.*56G=
XM_011538269.1:c.*56G=	XP_011536571.1:n.*56G=
XM_011538267.3:c.*156G=	XP_011536569.1:n.*156G=
XM_011538268.2:c.*56G=	XP_011536570.1:n.*56G=
XM_011538269.2:c.*56G=	XP_011536571.1:n.*56G=
NM_052845.4:c.*56G= MANE Select	NP_443077.1:n.*56G=
NR_038118.2:n.920G=