Canonical Allele Identifier: CA2062455145

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568857G= , CM000674.2:g.109568857G=	GRCh38
NC_000012.11:g.110006662G= , CM000674.1:g.110006662G=	GRCh37
NC_000012.10:g.108491045G=	NCBI36
NG_007096.1:g.9641C=
NG_007702.1:g.163G= , LRG_156:g.163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.203C= MANE Select	ENSP00000445920.1:p.Ser68=
ENST00000420167.6:c.*32C=	ENSP00000416136.2:n.*32C=
ENST00000503497.7:c.203C=	ENSP00000474881.1:p.Ser68=
ENST00000536760.1:n.206C=
ENST00000537236.2:c.203C=	ENSP00000483818.1:p.Ser68=
ENST00000537496.5:c.203C=	ENSP00000444793.1:p.Ser68=
ENST00000540016.5:c.135-3681C=	ENSP00000474582.1:n.135-3681C=
ENST00000541763.6:c.203C=	ENSP00000474981.1:p.Ser68=
ENST00000542390.5:n.230C=
ENST00000544051.5:c.141C=	ENSP00000438079.1:p.Phe47=
ENST00000545712.6:c.203C=	ENSP00000445920.1:p.Ser68=
NM_052845.3:c.203C=	NP_443077.1:p.Ser68=
NR_038118.1:n.276C=
XM_024448961.1:c.203C=	XP_024304729.1:p.Ser68=
NM_052845.4:c.203C= MANE Select	NP_443077.1:p.Ser68=
NR_038118.2:n.227C=