Canonical Allele Identifier: CA2062443946

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557000A= , CM000674.2:g.109557000A=	GRCh38
NC_000012.11:g.109994805A= , CM000674.1:g.109994805A=	GRCh37
NC_000012.10:g.108479188A=	NCBI36
NG_007096.1:g.21498T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*28T= MANE Select	ENSP00000445920.1:n.*28T=
ENST00000537496.5:c.*346T=	ENSP00000444793.1:n.*346T=
ENST00000540016.5:c.*28T=	ENSP00000474582.1:n.*28T=
ENST00000541763.6:c.1006T=	ENSP00000474981.1:n.1006T=
ENST00000544051.5:c.*662T=	ENSP00000438079.1:n.*662T=
ENST00000545712.6:c.*28T=	ENSP00000445920.1:n.*28T=
NM_052845.3:c.*28T=	NP_443077.1:n.*28T=
NR_038118.1:n.941T=
XM_011538266.1:c.*128T=	XP_011536568.1:n.*128T=
XM_011538267.1:c.*128T=	XP_011536569.1:n.*128T=
XM_011538268.1:c.*28T=	XP_011536570.1:n.*28T=
XM_011538269.1:c.*28T=	XP_011536571.1:n.*28T=
XM_011538267.3:c.*128T=	XP_011536569.1:n.*128T=
XM_011538268.2:c.*28T=	XP_011536570.1:n.*28T=
XM_011538269.2:c.*28T=	XP_011536571.1:n.*28T=
NM_052845.4:c.*28T= MANE Select	NP_443077.1:n.*28T=
NR_038118.2:n.892T=