Canonical Allele Identifier: CA386639449

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.110006586A>T (hg19) ; chr12:g.109568781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568781A>T , CM000674.2:g.109568781A>T	GRCh38
NC_000012.11:g.110006586A>T , CM000674.1:g.110006586A>T	GRCh37
NC_000012.10:g.108490969A>T	NCBI36
NG_007096.1:g.9717T>A
NG_007702.1:g.87A>T , LRG_156:g.87A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.279T>A MANE Select	ENSP00000445920.1:p.Ser93Arg
ENST00000420167.6:c.*108T>A	ENSP00000416136.2:n.*108T>A
ENST00000503497.7:c.279T>A	ENSP00000474881.1:p.Ser93Arg
ENST00000536760.1:n.282T>A
ENST00000537236.2:c.279T>A	ENSP00000483818.1:p.Ser93Arg
ENST00000537496.5:c.279T>A	ENSP00000444793.1:p.Ser93Arg
ENST00000540016.5:c.135-3605T>A	ENSP00000474582.1:n.135-3605T>A
ENST00000541763.6:c.279T>A	ENSP00000474981.1:p.Ser93Arg
ENST00000542390.5:n.306T>A
ENST00000544051.5:c.*73T>A	ENSP00000438079.1:n.*73T>A
ENST00000545712.6:c.279T>A	ENSP00000445920.1:p.Ser93Arg
NM_052845.3:c.279T>A	NP_443077.1:p.Ser93Arg
NR_038118.1:n.352T>A
XM_024448961.1:c.279T>A	XP_024304729.1:p.Ser93Arg
NM_052845.4:c.279T>A MANE Select	NP_443077.1:p.Ser93Arg
NR_038118.2:n.303T>A