Canonical Allele Identifier: CA2065371392

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982431T= , CM000674.2:g.115982431T=	GRCh38
NC_000012.11:g.116420236T= , CM000674.1:g.116420236T=	GRCh37
NC_000012.10:g.114904619T=	NCBI36
NG_023366.1:g.299756A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5128A= MANE Select	ENSP00000281928.3:p.Met1710=
ENST00000549786.2:c.4556A=
ENST00000648379.1:n.3496A=
ENST00000648737.1:n.4892A=
ENST00000648825.1:n.1868A=
ENST00000648916.1:n.3139A=
ENST00000649146.1:n.2371A=
ENST00000649607.1:c.3312A=
ENST00000649775.1:c.1617A=
ENST00000650226.1:c.5128A=	ENSP00000496981.1:p.Met1710=
ENST00000281928.7:c.5128A=	ENSP00000281928.3:p.Met1710=
ENST00000549786.1:c.492A=
ENST00000552340.1:c.160A=	ENSP00000449876.1:p.Met54=
NM_015335.4:c.5128A=	NP_056150.1:p.Met1710=
XM_011538080.1:c.5128A=	XP_011536382.1:p.Met1710=
XM_011538081.1:c.5125A=	XP_011536383.1:p.Met1709=
XM_011538082.1:c.5098A=	XP_011536384.1:p.Met1700=
XM_011538080.2:c.5128A=	XP_011536382.1:p.Met1710=
XM_011538081.2:c.5125A=	XP_011536383.1:p.Met1709=
XM_011538082.2:c.5098A=	XP_011536384.1:p.Met1700=
XM_017019090.1:c.5125A=	XP_016874579.1:p.Met1709=
NM_015335.5:c.5128A= MANE Select	NP_056150.1:p.Met1710=