Canonical Allele Identifier: CA2436355938
Gene: MED12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71132465G= , CM000685.2:g.71132465G= GRCh38
NC_000023.10:g.70352315G= , CM000685.1:g.70352315G= GRCh37
NC_000023.9:g.70269040G= NCBI36
NG_012808.1:g.18910G=

Transcript Alleles

HGVS Amino-acid Change
NM_005120.3:c.4342G= MANE Select NP_005111.2:p.Gly1448=
ENST00000374080.8:c.4342G= MANE Select ENSP00000363193.3:p.Gly1448=
NM_005120.2:c.4342G= NP_005111.2:p.Gly1448=
ENST00000333646.10:c.3883G= ENSP00000333125.7:p.Gly1295=
ENST00000333646.11:c.4222G= ENSP00000333125.8:p.Gly1408=
ENST00000374080.7:c.4342G= ENSP00000363193.3:p.Gly1448=
ENST00000374102.5:c.4342G= ENSP00000363215.1:p.Gly1448=
ENST00000374102.6:c.4342G= ENSP00000363215.2:p.Gly1448=
ENST00000685182.1:n.1145G=
ENST00000685655.1:c.295G= ENSP00000509298.1:p.Gly99=
ENST00000686169.1:n.719G=
ENST00000686548.1:c.*4238G= ENSP00000509582.1:n.*4238G=
ENST00000687161.1:n.1057G=
ENST00000687382.1:c.4342G= ENSP00000510724.1:p.Gly1448=
ENST00000687701.1:n.971G=
ENST00000688079.1:n.2337G=
ENST00000688663.1:c.*1263G= ENSP00000509348.1:n.*1263G=
ENST00000688881.1:n.996G=
ENST00000688993.1:n.713G=
ENST00000689768.1:n.2952G=
ENST00000690145.1:c.4342G= ENSP00000508818.1:p.Gly1448=
ENST00000690242.1:c.4342G= ENSP00000510090.1:p.Gly1448=
ENST00000690250.1:n.2011G=
ENST00000690690.1:c.795G=
ENST00000690828.1:n.4598G=
ENST00000691113.1:c.2821G= ENSP00000509755.1:n.2821G=
ENST00000691426.1:n.3641G=
ENST00000691468.1:c.4291G= ENSP00000509011.1:p.Gly1431=
ENST00000691909.1:n.1062G=
ENST00000692304.1:c.4342G= ENSP00000508427.1:p.Gly1448=
ENST00000692893.1:n.1651G=
ENST00000692964.1:n.1176G=
ENST00000693050.1:n.1019G=
ENST00000693324.1:c.4306G= ENSP00000508643.1:p.Gly1436=
ENST00000693391.1:c.2287G= ENSP00000509563.1:p.Gly763=
XM_005262317.1:c.4342G= XP_005262374.1:p.Gly1448=
XM_005262319.1:c.4342G= XP_005262376.1:p.Gly1448=