Canonical Allele Identifier: CA2062448097

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561039C= , CM000674.2:g.109561039C=	GRCh38
NC_000012.11:g.109998844C= , CM000674.1:g.109998844C=	GRCh37
NC_000012.10:g.108483227C=	NCBI36
NG_007096.1:g.17459G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.584+1G= MANE Select	ENSP00000445920.1:n.584+1G=
ENST00000537496.5:c.*149+1G=	ENSP00000444793.1:n.*149+1G=
ENST00000540016.5:c.428+1G=	ENSP00000474582.1:n.428+1G=
ENST00000541763.6:c.809+1G=	ENSP00000474981.1:n.809+1G=
ENST00000544051.5:c.*465+1G=	ENSP00000438079.1:n.*465+1G=
ENST00000545712.6:c.584+1G=	ENSP00000445920.1:n.584+1G=
NM_052845.3:c.584+1G=	NP_443077.1:n.584+1G=
NR_038118.1:n.744+1G=
XM_011538266.1:c.429+1G=	XP_011536568.1:n.429+1G=
XM_011538267.1:c.429+1G=	XP_011536569.1:n.429+1G=
XM_011538268.1:c.311+1G=	XP_011536570.1:n.311+1G=
XM_011538269.1:c.308+1G=	XP_011536571.1:n.308+1G=
XM_011538267.3:c.429+1G=	XP_011536569.1:n.429+1G=
XM_011538268.2:c.311+1G=	XP_011536570.1:n.311+1G=
XM_011538269.2:c.308+1G=	XP_011536571.1:n.308+1G=
XM_024448961.1:c.584+1G=	XP_024304729.1:n.584+1G=
NM_052845.4:c.584+1G= MANE Select	NP_443077.1:n.584+1G=
NR_038118.2:n.695+1G=