Canonical Allele Identifier: CA516716683

Gene: MED12

Linked Data

• MyVariant Identifiers: chrX:g.70344151T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71124301T>C , CM000685.2:g.71124301T>C	GRCh38
NC_000023.10:g.70344151T>C , CM000685.1:g.70344151T>C	GRCh37
NC_000023.9:g.70260876T>C	NCBI36
NG_012808.1:g.10746T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333646.11:c.1767T>C	ENSP00000333125.8:p.Pro589=
ENST00000374102.6:c.1887T>C	ENSP00000363215.2:p.Pro629=
ENST00000686548.1:c.*1783T>C	ENSP00000509582.1:n.*1783T>C
ENST00000687382.1:c.1887T>C	ENSP00000510724.1:p.Pro629=
ENST00000688663.1:c.1887T>C	ENSP00000509348.1:p.Pro629=
ENST00000689008.1:c.*2221T>C	ENSP00000509134.1:n.*2221T>C
ENST00000689768.1:n.497T>C
ENST00000690145.1:c.1887T>C	ENSP00000508818.1:p.Pro629=
ENST00000690242.1:c.1887T>C	ENSP00000510090.1:p.Pro629=
ENST00000690828.1:n.2043T>C
ENST00000691385.1:n.1165T>C
ENST00000691426.1:n.118T>C
ENST00000691468.1:c.1887T>C	ENSP00000509011.1:p.Pro629=
ENST00000692304.1:c.1887T>C	ENSP00000508427.1:p.Pro629=
ENST00000692864.1:c.*2221T>C	ENSP00000510321.1:n.*2221T>C
ENST00000693324.1:c.1887T>C	ENSP00000508643.1:p.Pro629=
ENST00000374080.8:c.1887T>C MANE Select	ENSP00000363193.3:p.Pro629=
ENST00000333646.10:c.1428T>C	ENSP00000333125.7:p.Pro476=
ENST00000374080.7:c.1887T>C	ENSP00000363193.3:p.Pro629=
ENST00000374102.5:c.1887T>C	ENSP00000363215.1:p.Pro629=
NM_005120.2:c.1887T>C	NP_005111.2:p.Pro629=
XM_005262317.1:c.1887T>C	XP_005262374.1:p.Pro629=
XM_005262319.1:c.1887T>C	XP_005262376.1:p.Pro629=
NM_005120.3:c.1887T>C MANE Select	NP_005111.2:p.Pro629=