Canonical Allele Identifier: CA481710114

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994905T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557100T>A , CM000674.2:g.109557100T>A	GRCh38
NC_000012.11:g.109994905T>A , CM000674.1:g.109994905T>A	GRCh37
NC_000012.10:g.108479288T>A	NCBI36
NG_007096.1:g.21398A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.681A>T MANE Select	ENSP00000445920.1:p.Ala227=
ENST00000537496.5:c.*246A>T	ENSP00000444793.1:n.*246A>T
ENST00000540016.5:c.525A>T	ENSP00000474582.1:p.Ala175=
ENST00000541763.6:c.906A>T	ENSP00000474981.1:n.906A>T
ENST00000544051.5:c.*562A>T	ENSP00000438079.1:n.*562A>T
ENST00000545712.6:c.681A>T	ENSP00000445920.1:p.Ala227=
NM_052845.3:c.681A>T	NP_443077.1:p.Ala227=
NR_038118.1:n.841A>T
XM_011538266.1:c.*28A>T	XP_011536568.1:n.*28A>T
XM_011538267.1:c.*28A>T	XP_011536569.1:n.*28A>T
XM_011538268.1:c.408A>T	XP_011536570.1:p.Ala136=
XM_011538269.1:c.405A>T	XP_011536571.1:p.Ala135=
XM_011538267.3:c.*28A>T	XP_011536569.1:n.*28A>T
XM_011538268.2:c.408A>T	XP_011536570.1:p.Ala136=
XM_011538269.2:c.405A>T	XP_011536571.1:p.Ala135=
NM_052845.4:c.681A>T MANE Select	NP_443077.1:p.Ala227=
NR_038118.2:n.792A>T