Canonical Allele Identifier: CA2062455009

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568681C= , CM000674.2:g.109568681C=	GRCh38
NC_000012.11:g.110006486C= , CM000674.1:g.110006486C=	GRCh37
NC_000012.10:g.108490869C=	NCBI36
NG_007096.1:g.9817G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.290+89G= MANE Select	ENSP00000445920.1:n.290+89G=
ENST00000420167.6:c.*119+89G=	ENSP00000416136.2:n.*119+89G=
ENST00000503497.7:c.290+89G=	ENSP00000474881.1:n.290+89G=
ENST00000536760.1:n.293+89G=
ENST00000537236.2:c.*85G=	ENSP00000483818.1:n.*85G=
ENST00000537496.5:c.290+89G=	ENSP00000444793.1:n.290+89G=
ENST00000540016.5:c.135-3505G=	ENSP00000474582.1:n.135-3505G=
ENST00000541763.6:c.290+89G=	ENSP00000474981.1:n.290+89G=
ENST00000542390.5:n.317+89G=
ENST00000544051.5:c.*84+89G=	ENSP00000438079.1:n.*84+89G=
ENST00000545712.6:c.290+89G=	ENSP00000445920.1:n.290+89G=
NM_052845.3:c.290+89G=	NP_443077.1:n.290+89G=
NR_038118.1:n.363+89G=
XM_011538266.1:c.-379G=	XP_011536568.1:n.-379G=
XM_011538267.1:c.-268G=	XP_011536569.1:n.-268G=
XM_011538269.1:c.-413G=	XP_011536571.1:n.-413G=
XM_011538267.3:c.-268G=	XP_011536569.1:n.-268G=
XM_011538269.2:c.-413G=	XP_011536571.1:n.-413G=
XM_024448961.1:c.290+89G=	XP_024304729.1:n.290+89G=
NM_052845.4:c.290+89G= MANE Select	NP_443077.1:n.290+89G=
NR_038118.2:n.314+89G=