Canonical Allele Identifier: CA2062455028

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568705A= , CM000674.2:g.109568705A=	GRCh38
NC_000012.11:g.110006510A= , CM000674.1:g.110006510A=	GRCh37
NC_000012.10:g.108490893A=	NCBI36
NG_007096.1:g.9793T=
NG_007702.1:g.11A= , LRG_156:g.11A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.290+65T= MANE Select	ENSP00000445920.1:n.290+65T=
ENST00000420167.6:c.*119+65T=	ENSP00000416136.2:n.*119+65T=
ENST00000503497.7:c.290+65T=	ENSP00000474881.1:n.290+65T=
ENST00000536760.1:n.293+65T=
ENST00000537236.2:c.*61T=	ENSP00000483818.1:n.*61T=
ENST00000537496.5:c.290+65T=	ENSP00000444793.1:n.290+65T=
ENST00000540016.5:c.135-3529T=	ENSP00000474582.1:n.135-3529T=
ENST00000541763.6:c.290+65T=	ENSP00000474981.1:n.290+65T=
ENST00000542390.5:n.317+65T=
ENST00000544051.5:c.*84+65T=	ENSP00000438079.1:n.*84+65T=
ENST00000545712.6:c.290+65T=	ENSP00000445920.1:n.290+65T=
NM_052845.3:c.290+65T=	NP_443077.1:n.290+65T=
NR_038118.1:n.363+65T=
XM_011538266.1:c.-403T=	XP_011536568.1:n.-403T=
XM_011538267.1:c.-292T=	XP_011536569.1:n.-292T=
XM_011538269.1:c.-437T=	XP_011536571.1:n.-437T=
XM_011538267.3:c.-292T=	XP_011536569.1:n.-292T=
XM_011538269.2:c.-437T=	XP_011536571.1:n.-437T=
XM_024448961.1:c.290+65T=	XP_024304729.1:n.290+65T=
NM_052845.4:c.290+65T= MANE Select	NP_443077.1:n.290+65T=
NR_038118.2:n.314+65T=