Canonical Allele Identifier: CA2062455016

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568689C= , CM000674.2:g.109568689C=	GRCh38
NC_000012.11:g.110006494C= , CM000674.1:g.110006494C=	GRCh37
NC_000012.10:g.108490877C=	NCBI36
NG_007096.1:g.9809G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.290+81G= MANE Select	ENSP00000445920.1:n.290+81G=
ENST00000420167.6:c.*119+81G=	ENSP00000416136.2:n.*119+81G=
ENST00000503497.7:c.290+81G=	ENSP00000474881.1:n.290+81G=
ENST00000536760.1:n.293+81G=
ENST00000537236.2:c.*77G=	ENSP00000483818.1:n.*77G=
ENST00000537496.5:c.290+81G=	ENSP00000444793.1:n.290+81G=
ENST00000540016.5:c.135-3513G=	ENSP00000474582.1:n.135-3513G=
ENST00000541763.6:c.290+81G=	ENSP00000474981.1:n.290+81G=
ENST00000542390.5:n.317+81G=
ENST00000544051.5:c.*84+81G=	ENSP00000438079.1:n.*84+81G=
ENST00000545712.6:c.290+81G=	ENSP00000445920.1:n.290+81G=
NM_052845.3:c.290+81G=	NP_443077.1:n.290+81G=
NR_038118.1:n.363+81G=
XM_011538266.1:c.-387G=	XP_011536568.1:n.-387G=
XM_011538267.1:c.-276G=	XP_011536569.1:n.-276G=
XM_011538269.1:c.-421G=	XP_011536571.1:n.-421G=
XM_011538267.3:c.-276G=	XP_011536569.1:n.-276G=
XM_011538269.2:c.-421G=	XP_011536571.1:n.-421G=
XM_024448961.1:c.290+81G=	XP_024304729.1:n.290+81G=
NM_052845.4:c.290+81G= MANE Select	NP_443077.1:n.290+81G=
NR_038118.2:n.314+81G=