Canonical Allele Identifier: CA413509885

Gene: MED12

Linked Data

• COSMIC: COSM3563075 ; COSM3563076
• MyVariant Identifiers: chrX:g.70344182C>T (hg19) ; chrX:g.71124332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71124332C>T , CM000685.2:g.71124332C>T	GRCh38
NC_000023.10:g.70344182C>T , CM000685.1:g.70344182C>T	GRCh37
NC_000023.9:g.70260907C>T	NCBI36
NG_012808.1:g.10777C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333646.11:c.1798C>T	ENSP00000333125.8:p.Pro600Ser
ENST00000374102.6:c.1918C>T	ENSP00000363215.2:p.Pro640Ser
ENST00000686548.1:c.*1814C>T	ENSP00000509582.1:n.*1814C>T
ENST00000687382.1:c.1918C>T	ENSP00000510724.1:p.Pro640Ser
ENST00000688663.1:c.1918C>T	ENSP00000509348.1:p.Pro640Ser
ENST00000689008.1:c.*2252C>T	ENSP00000509134.1:n.*2252C>T
ENST00000689768.1:n.528C>T
ENST00000690145.1:c.1918C>T	ENSP00000508818.1:p.Pro640Ser
ENST00000690242.1:c.1918C>T	ENSP00000510090.1:p.Pro640Ser
ENST00000690828.1:n.2074C>T
ENST00000691385.1:n.1196C>T
ENST00000691426.1:n.149C>T
ENST00000691468.1:c.1918C>T	ENSP00000509011.1:p.Pro640Ser
ENST00000692304.1:c.1918C>T	ENSP00000508427.1:p.Pro640Ser
ENST00000692864.1:c.*2252C>T	ENSP00000510321.1:n.*2252C>T
ENST00000693324.1:c.1918C>T	ENSP00000508643.1:p.Pro640Ser
ENST00000374080.8:c.1918C>T MANE Select	ENSP00000363193.3:p.Pro640Ser
ENST00000333646.10:c.1459C>T	ENSP00000333125.7:p.Pro487Ser
ENST00000374080.7:c.1918C>T	ENSP00000363193.3:p.Pro640Ser
ENST00000374102.5:c.1918C>T	ENSP00000363215.1:p.Pro640Ser
NM_005120.2:c.1918C>T	NP_005111.2:p.Pro640Ser
XM_005262317.1:c.1918C>T	XP_005262374.1:p.Pro640Ser
XM_005262319.1:c.1918C>T	XP_005262376.1:p.Pro640Ser
NM_005120.3:c.1918C>T MANE Select	NP_005111.2:p.Pro640Ser