Canonical Allele Identifier: CA912973414

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109998844dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561040dup , CM000674.2:g.109561040dup	GRCh38
NC_000012.11:g.109998845dup , CM000674.1:g.109998845dup	GRCh37
NC_000012.10:g.108483228dup	NCBI36
NG_007096.1:g.17459dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.584+1dup
ENST00000537496.5:c.*149+1dup
ENST00000540016.5:c.428+1dup
ENST00000541763.6:c.809+1dup
ENST00000544051.5:c.*465+1dup
ENST00000545712.6:c.584+1dup
NM_052845.3:c.584+1dup
NR_038118.1:n.744+1dup
XM_011538266.1:c.429+1dup
XM_011538267.1:c.429+1dup
XM_011538268.1:c.311+1dup
XM_011538269.1:c.308+1dup
XM_011538267.3:c.429+1dup
XM_011538268.2:c.311+1dup
XM_011538269.2:c.308+1dup
XM_024448961.1:c.584+1dup
NM_052845.4:c.584+1dup
NR_038118.2:n.695+1dup