Canonical Allele Identifier: CA2062458455

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109573248C= , CM000674.2:g.109573248C=	GRCh38
NC_000012.11:g.110011053C= , CM000674.1:g.110011053C=	GRCh37
NC_000012.10:g.108495436C=	NCBI36
NG_007096.1:g.5250G=
NG_007702.1:g.4554C= , LRG_156:g.4554C=

Transcript Alleles

HGVS	Amino-acid Change
NM_052845.4:c.134+99G= MANE Select	NP_443077.1:n.134+99G=
ENST00000545712.7:c.134+99G= MANE Select	ENSP00000445920.1:n.134+99G=
NM_052845.3:c.134+99G=	NP_443077.1:n.134+99G=
NR_038118.1:n.207+99G=
NR_038118.2:n.158+99G=
ENST00000420167.6:c.134+99G=	ENSP00000416136.2:n.134+99G=
ENST00000503497.7:c.134+99G=	ENSP00000474881.1:n.134+99G=
ENST00000536760.1:n.137+99G=
ENST00000537236.2:c.134+99G=	ENSP00000483818.1:n.134+99G=
ENST00000537496.5:c.134+99G=	ENSP00000444793.1:n.134+99G=
ENST00000540016.5:c.134+99G=	ENSP00000474582.1:n.134+99G=
ENST00000541763.6:c.134+99G=	ENSP00000474981.1:n.134+99G=
ENST00000542390.5:n.161+99G=
ENST00000544051.5:c.134+99G=	ENSP00000438079.1:n.134+99G=
ENST00000545712.6:c.134+99G=	ENSP00000445920.1:n.134+99G=
XM_024448961.1:c.134+99G=	XP_024304729.1:n.134+99G=