Canonical Allele Identifier: CA2062443953

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557005C= , CM000674.2:g.109557005C=	GRCh38
NC_000012.11:g.109994810C= , CM000674.1:g.109994810C=	GRCh37
NC_000012.10:g.108479193C=	NCBI36
NG_007096.1:g.21493G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*23G= MANE Select	ENSP00000445920.1:n.*23G=
ENST00000537496.5:c.*341G=	ENSP00000444793.1:n.*341G=
ENST00000540016.5:c.*23G=	ENSP00000474582.1:n.*23G=
ENST00000541763.6:c.1001G=	ENSP00000474981.1:n.1001G=
ENST00000544051.5:c.*657G=	ENSP00000438079.1:n.*657G=
ENST00000545712.6:c.*23G=	ENSP00000445920.1:n.*23G=
NM_052845.3:c.*23G=	NP_443077.1:n.*23G=
NR_038118.1:n.936G=
XM_011538266.1:c.*123G=	XP_011536568.1:n.*123G=
XM_011538267.1:c.*123G=	XP_011536569.1:n.*123G=
XM_011538268.1:c.*23G=	XP_011536570.1:n.*23G=
XM_011538269.1:c.*23G=	XP_011536571.1:n.*23G=
XM_011538267.3:c.*123G=	XP_011536569.1:n.*123G=
XM_011538268.2:c.*23G=	XP_011536570.1:n.*23G=
XM_011538269.2:c.*23G=	XP_011536571.1:n.*23G=
NM_052845.4:c.*23G= MANE Select	NP_443077.1:n.*23G=
NR_038118.2:n.887G=