Canonical Allele Identifier: CA2436354504

Gene: MED12

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71127931A= , CM000685.2:g.71127931A=	GRCh38
NC_000023.10:g.70347781A= , CM000685.1:g.70347781A=	GRCh37
NC_000023.9:g.70264506A=	NCBI36
NG_012808.1:g.14376A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333646.11:c.2900A=	ENSP00000333125.8:p.Asn967=
ENST00000374102.6:c.3020A=	ENSP00000363215.2:p.Asn1007=
ENST00000489199.2:c.39A=
ENST00000686548.1:c.*2916A=	ENSP00000509582.1:n.*2916A=
ENST00000687382.1:c.3020A=	ENSP00000510724.1:p.Asn1007=
ENST00000688079.1:n.1015A=
ENST00000688663.1:c.3020A=	ENSP00000509348.1:p.Asn1007=
ENST00000689768.1:n.1630A=
ENST00000690145.1:c.3020A=	ENSP00000508818.1:p.Asn1007=
ENST00000690242.1:c.3020A=	ENSP00000510090.1:p.Asn1007=
ENST00000690250.1:n.22A=
ENST00000690828.1:n.3176A=
ENST00000691113.1:c.1499A=	ENSP00000509755.1:n.1499A=
ENST00000691426.1:n.1676A=
ENST00000691468.1:c.2969A=	ENSP00000509011.1:p.Asn990=
ENST00000692304.1:c.3020A=	ENSP00000508427.1:p.Asn1007=
ENST00000693324.1:c.2984A=	ENSP00000508643.1:p.Asn995=
ENST00000693391.1:c.965A=	ENSP00000509563.1:p.Asn322=
ENST00000374080.8:c.3020A= MANE Select	ENSP00000363193.3:p.Asn1007=
ENST00000333646.10:c.2561A=	ENSP00000333125.7:p.Asn854=
ENST00000374080.7:c.3020A=	ENSP00000363193.3:p.Asn1007=
ENST00000374102.5:c.3020A=	ENSP00000363215.1:p.Asn1007=
NM_005120.2:c.3020A=	NP_005111.2:p.Asn1007=
XM_005262317.1:c.3020A=	XP_005262374.1:p.Asn1007=
XM_005262319.1:c.3020A=	XP_005262376.1:p.Asn1007=
NM_005120.3:c.3020A= MANE Select	NP_005111.2:p.Asn1007=