Canonical Allele Identifier: CA481712493

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.110006639T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568834T>G , CM000674.2:g.109568834T>G	GRCh38
NC_000012.11:g.110006639T>G , CM000674.1:g.110006639T>G	GRCh37
NC_000012.10:g.108491022T>G	NCBI36
NG_007096.1:g.9664A>C
NG_007702.1:g.140T>G , LRG_156:g.140T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.226A>C MANE Select	ENSP00000445920.1:p.Arg76=
ENST00000420167.6:c.*55A>C	ENSP00000416136.2:n.*55A>C
ENST00000503497.7:c.226A>C	ENSP00000474881.1:p.Arg76=
ENST00000536760.1:n.229A>C
ENST00000537236.2:c.226A>C	ENSP00000483818.1:p.Arg76=
ENST00000537496.5:c.226A>C	ENSP00000444793.1:p.Arg76=
ENST00000540016.5:c.135-3658A>C	ENSP00000474582.1:n.135-3658A>C
ENST00000541763.6:c.226A>C	ENSP00000474981.1:p.Arg76=
ENST00000542390.5:n.253A>C
ENST00000544051.5:c.*20A>C	ENSP00000438079.1:n.*20A>C
ENST00000545712.6:c.226A>C	ENSP00000445920.1:p.Arg76=
NM_052845.3:c.226A>C	NP_443077.1:p.Arg76=
NR_038118.1:n.299A>C
XM_024448961.1:c.226A>C	XP_024304729.1:p.Arg76=
NM_052845.4:c.226A>C MANE Select	NP_443077.1:p.Arg76=
NR_038118.2:n.250A>C