Canonical Allele Identifier: CA2065372470

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982925A= , CM000674.2:g.115982925A=	GRCh38
NC_000012.11:g.116420730A= , CM000674.1:g.116420730A=	GRCh37
NC_000012.10:g.114905113A=	NCBI36
NG_023366.1:g.299262T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4955+192T= MANE Select	ENSP00000281928.3:n.4955+192T=
ENST00000549786.2:c.4383+192T=
ENST00000648379.1:n.3323+192T=
ENST00000648737.1:n.4719+192T=
ENST00000648825.1:n.1695+192T=
ENST00000648916.1:n.2966+192T=
ENST00000649146.1:n.1877T=
ENST00000649607.1:c.3139+192T=
ENST00000649775.1:c.1452+192T=
ENST00000650226.1:c.4955+192T=	ENSP00000496981.1:n.4955+192T=
ENST00000281928.7:c.4955+192T=	ENSP00000281928.3:n.4955+192T=
ENST00000549786.1:c.319+192T=
NM_015335.4:c.4955+192T=	NP_056150.1:n.4955+192T=
XM_011538080.1:c.4955+192T=	XP_011536382.1:n.4955+192T=
XM_011538081.1:c.4952+192T=	XP_011536383.1:n.4952+192T=
XM_011538082.1:c.4925+192T=	XP_011536384.1:n.4925+192T=
XM_011538080.2:c.4955+192T=	XP_011536382.1:n.4955+192T=
XM_011538081.2:c.4952+192T=	XP_011536383.1:n.4952+192T=
XM_011538082.2:c.4925+192T=	XP_011536384.1:n.4925+192T=
XM_017019090.1:c.4952+192T=	XP_016874579.1:n.4952+192T=
NM_015335.5:c.4955+192T= MANE Select	NP_056150.1:n.4955+192T=