Canonical Allele Identifier: CA481709986

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994848C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557043C>T , CM000674.2:g.109557043C>T	GRCh38
NC_000012.11:g.109994848C>T , CM000674.1:g.109994848C>T	GRCh37
NC_000012.10:g.108479231C>T	NCBI36
NG_007096.1:g.21455G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.738G>A MANE Select	ENSP00000445920.1:p.Glu246=
ENST00000537496.5:c.*303G>A	ENSP00000444793.1:n.*303G>A
ENST00000540016.5:c.582G>A	ENSP00000474582.1:p.Glu194=
ENST00000541763.6:c.963G>A	ENSP00000474981.1:n.963G>A
ENST00000544051.5:c.*619G>A	ENSP00000438079.1:n.*619G>A
ENST00000545712.6:c.738G>A	ENSP00000445920.1:p.Glu246=
NM_052845.3:c.738G>A	NP_443077.1:p.Glu246=
NR_038118.1:n.898G>A
XM_011538266.1:c.*85G>A	XP_011536568.1:n.*85G>A
XM_011538267.1:c.*85G>A	XP_011536569.1:n.*85G>A
XM_011538268.1:c.465G>A	XP_011536570.1:p.Glu155=
XM_011538269.1:c.462G>A	XP_011536571.1:p.Glu154=
XM_011538267.3:c.*85G>A	XP_011536569.1:n.*85G>A
XM_011538268.2:c.465G>A	XP_011536570.1:p.Glu155=
XM_011538269.2:c.462G>A	XP_011536571.1:p.Glu154=
NM_052845.4:c.738G>A MANE Select	NP_443077.1:p.Glu246=
NR_038118.2:n.849G>A