Canonical Allele Identifier: CA386639624

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.110006626T>C (hg19) ; chr12:g.109568821T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568821T>C , CM000674.2:g.109568821T>C	GRCh38
NC_000012.11:g.110006626T>C , CM000674.1:g.110006626T>C	GRCh37
NC_000012.10:g.108491009T>C	NCBI36
NG_007096.1:g.9677A>G
NG_007702.1:g.127T>C , LRG_156:g.127T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.239A>G MANE Select	ENSP00000445920.1:p.Asp80Gly
ENST00000420167.6:c.*68A>G	ENSP00000416136.2:n.*68A>G
ENST00000503497.7:c.239A>G	ENSP00000474881.1:p.Asp80Gly
ENST00000536760.1:n.242A>G
ENST00000537236.2:c.239A>G	ENSP00000483818.1:p.Asp80Gly
ENST00000537496.5:c.239A>G	ENSP00000444793.1:p.Asp80Gly
ENST00000540016.5:c.135-3645A>G	ENSP00000474582.1:n.135-3645A>G
ENST00000541763.6:c.239A>G	ENSP00000474981.1:p.Asp80Gly
ENST00000542390.5:n.266A>G
ENST00000544051.5:c.*33A>G	ENSP00000438079.1:n.*33A>G
ENST00000545712.6:c.239A>G	ENSP00000445920.1:p.Asp80Gly
NM_052845.3:c.239A>G	NP_443077.1:p.Asp80Gly
NR_038118.1:n.312A>G
XM_024448961.1:c.239A>G	XP_024304729.1:p.Asp80Gly
NM_052845.4:c.239A>G MANE Select	NP_443077.1:p.Asp80Gly
NR_038118.2:n.263A>G