Canonical Allele Identifier: CA413509954
Gene: MED12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71124343C>A , CM000685.2:g.71124343C>A GRCh38
NC_000023.10:g.70344193C>A , CM000685.1:g.70344193C>A GRCh37
NC_000023.9:g.70260918C>A NCBI36
NG_012808.1:g.10788C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333646.11:c.1809C>A ENSP00000333125.8:p.Asp603Glu
ENST00000374102.6:c.1929C>A ENSP00000363215.2:p.Asp643Glu
ENST00000686548.1:c.*1825C>A ENSP00000509582.1:n.*1825C>A
ENST00000687382.1:c.1929C>A ENSP00000510724.1:p.Asp643Glu
ENST00000688663.1:c.1929C>A ENSP00000509348.1:p.Asp643Glu
ENST00000689008.1:c.*2263C>A ENSP00000509134.1:n.*2263C>A
ENST00000689768.1:n.539C>A
ENST00000690145.1:c.1929C>A ENSP00000508818.1:p.Asp643Glu
ENST00000690242.1:c.1929C>A ENSP00000510090.1:p.Asp643Glu
ENST00000690828.1:n.2085C>A
ENST00000691385.1:n.1207C>A
ENST00000691426.1:n.160C>A
ENST00000691468.1:c.1929C>A ENSP00000509011.1:p.Asp643Glu
ENST00000692304.1:c.1929C>A ENSP00000508427.1:p.Asp643Glu
ENST00000692864.1:c.*2263C>A ENSP00000510321.1:n.*2263C>A
ENST00000693324.1:c.1929C>A ENSP00000508643.1:p.Asp643Glu
ENST00000374080.8:c.1929C>A MANE Select ENSP00000363193.3:p.Asp643Glu
ENST00000333646.10:c.1470C>A ENSP00000333125.7:p.Asp490Glu
ENST00000374080.7:c.1929C>A ENSP00000363193.3:p.Asp643Glu
ENST00000374102.5:c.1929C>A ENSP00000363215.1:p.Asp643Glu
NM_005120.2:c.1929C>A NP_005111.2:p.Asp643Glu
XM_005262317.1:c.1929C>A XP_005262374.1:p.Asp643Glu
XM_005262319.1:c.1929C>A XP_005262376.1:p.Asp643Glu
NM_005120.3:c.1929C>A MANE Select NP_005111.2:p.Asp643Glu