Canonical Allele Identifier: CA2065410887

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970613A= , CM000674.2:g.115970613A=	GRCh38
NC_000012.11:g.116408418A= , CM000674.1:g.116408418A=	GRCh37
NC_000012.10:g.114892801A=	NCBI36
NG_023366.1:g.311574T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6048T= MANE Select	ENSP00000281928.3:p.Asp2016=
ENST00000548784.2:n.2262T=
ENST00000648379.1:n.4416T=
ENST00000648737.1:n.5812T=
ENST00000648825.1:n.4233T=
ENST00000648916.1:n.4059T=
ENST00000649607.1:c.4232T=
ENST00000649775.1:c.2537T=
ENST00000650226.1:c.6084T=	ENSP00000496981.1:p.Asp2028=
ENST00000281928.7:c.6048T=	ENSP00000281928.3:p.Asp2016=
NM_015335.4:c.6048T=	NP_056150.1:p.Asp2016=
XM_011538080.1:c.6084T=	XP_011536382.1:p.Asp2028=
XM_011538081.1:c.6081T=	XP_011536383.1:p.Asp2027=
XM_011538082.1:c.6054T=	XP_011536384.1:p.Asp2018=
XM_011538080.2:c.6084T=	XP_011536382.1:p.Asp2028=
XM_011538081.2:c.6081T=	XP_011536383.1:p.Asp2027=
XM_011538082.2:c.6054T=	XP_011536384.1:p.Asp2018=
XM_017019090.1:c.6045T=	XP_016874579.1:p.Asp2015=
NM_015335.5:c.6048T= MANE Select	NP_056150.1:p.Asp2016=