Canonical Allele Identifier: CA2065372390

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982875A= , CM000674.2:g.115982875A=	GRCh38
NC_000012.11:g.116420680A= , CM000674.1:g.116420680A=	GRCh37
NC_000012.10:g.114905063A=	NCBI36
NG_023366.1:g.299312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4955+242T= MANE Select	ENSP00000281928.3:n.4955+242T=
ENST00000549786.2:c.4383+242T=
ENST00000648379.1:n.3323+242T=
ENST00000648737.1:n.4719+242T=
ENST00000648825.1:n.1695+242T=
ENST00000648916.1:n.2966+242T=
ENST00000649146.1:n.1927T=
ENST00000649607.1:c.3139+242T=
ENST00000649775.1:c.1452+242T=
ENST00000650226.1:c.4955+242T=	ENSP00000496981.1:n.4955+242T=
ENST00000281928.7:c.4955+242T=	ENSP00000281928.3:n.4955+242T=
ENST00000549786.1:c.319+242T=
NM_015335.4:c.4955+242T=	NP_056150.1:n.4955+242T=
XM_011538080.1:c.4955+242T=	XP_011536382.1:n.4955+242T=
XM_011538081.1:c.4952+242T=	XP_011536383.1:n.4952+242T=
XM_011538082.1:c.4925+242T=	XP_011536384.1:n.4925+242T=
XM_011538080.2:c.4955+242T=	XP_011536382.1:n.4955+242T=
XM_011538081.2:c.4952+242T=	XP_011536383.1:n.4952+242T=
XM_011538082.2:c.4925+242T=	XP_011536384.1:n.4925+242T=
XM_017019090.1:c.4952+242T=	XP_016874579.1:n.4952+242T=
NM_015335.5:c.4955+242T= MANE Select	NP_056150.1:n.4955+242T=