Canonical Allele Identifier: CA2062444513

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557404C= , CM000674.2:g.109557404C=	GRCh38
NC_000012.11:g.109995209C= , CM000674.1:g.109995209C=	GRCh37
NC_000012.10:g.108479592C=	NCBI36
NG_007096.1:g.21094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-268G= MANE Select	ENSP00000445920.1:n.645-268G=
ENST00000537496.5:c.*210-268G=	ENSP00000444793.1:n.*210-268G=
ENST00000540016.5:c.489-268G=	ENSP00000474582.1:n.489-268G=
ENST00000541763.6:c.870-268G=	ENSP00000474981.1:n.870-268G=
ENST00000544051.5:c.*526-268G=	ENSP00000438079.1:n.*526-268G=
ENST00000545712.6:c.645-268G=	ENSP00000445920.1:n.645-268G=
NM_052845.3:c.645-268G=	NP_443077.1:n.645-268G=
NR_038118.1:n.805-268G=
XM_011538266.1:c.490-268G=	XP_011536568.1:n.490-268G=
XM_011538267.1:c.490-268G=	XP_011536569.1:n.490-268G=
XM_011538268.1:c.372-268G=	XP_011536570.1:n.372-268G=
XM_011538269.1:c.369-268G=	XP_011536571.1:n.369-268G=
XM_011538267.3:c.490-268G=	XP_011536569.1:n.490-268G=
XM_011538268.2:c.372-268G=	XP_011536570.1:n.372-268G=
XM_011538269.2:c.369-268G=	XP_011536571.1:n.369-268G=
NM_052845.4:c.645-268G= MANE Select	NP_443077.1:n.645-268G=
NR_038118.2:n.756-268G=