Canonical Allele Identifier: CA2062443936

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109556992A= , CM000674.2:g.109556992A=	GRCh38
NC_000012.11:g.109994797A= , CM000674.1:g.109994797A=	GRCh37
NC_000012.10:g.108479180A=	NCBI36
NG_007096.1:g.21506T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*36T= MANE Select	ENSP00000445920.1:n.*36T=
ENST00000537496.5:c.*354T=	ENSP00000444793.1:n.*354T=
ENST00000540016.5:c.*36T=	ENSP00000474582.1:n.*36T=
ENST00000541763.6:c.1014T=	ENSP00000474981.1:n.1014T=
ENST00000544051.5:c.*670T=	ENSP00000438079.1:n.*670T=
ENST00000545712.6:c.*36T=	ENSP00000445920.1:n.*36T=
NM_052845.3:c.*36T=	NP_443077.1:n.*36T=
NR_038118.1:n.949T=
XM_011538266.1:c.*136T=	XP_011536568.1:n.*136T=
XM_011538267.1:c.*136T=	XP_011536569.1:n.*136T=
XM_011538268.1:c.*36T=	XP_011536570.1:n.*36T=
XM_011538269.1:c.*36T=	XP_011536571.1:n.*36T=
XM_011538267.3:c.*136T=	XP_011536569.1:n.*136T=
XM_011538268.2:c.*36T=	XP_011536570.1:n.*36T=
XM_011538269.2:c.*36T=	XP_011536571.1:n.*36T=
NM_052845.4:c.*36T= MANE Select	NP_443077.1:n.*36T=
NR_038118.2:n.900T=