Canonical Allele Identifier: CA2065396942

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997221T= , CM000674.2:g.115997221T=	GRCh38
NC_000012.11:g.116435026T= , CM000674.1:g.116435026T=	GRCh37
NC_000012.10:g.114919409T=	NCBI36
NG_023366.1:g.284966A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2579A= MANE Select	ENSP00000281928.3:p.Asp860=
ENST00000548743.2:c.2549A=	ENSP00000448553.2:p.Asp850=
ENST00000549786.2:c.2007A=
ENST00000647927.1:n.2952A=
ENST00000648173.1:n.1374A=
ENST00000648379.1:n.947A=
ENST00000648737.1:n.2343A=
ENST00000648916.1:n.590A=
ENST00000649607.1:c.763A=
ENST00000650226.1:c.2579A=	ENSP00000496981.1:p.Asp860=
ENST00000281928.7:c.2579A=	ENSP00000281928.3:p.Asp860=
NM_015335.4:c.2579A=	NP_056150.1:p.Asp860=
XM_011538080.1:c.2579A=	XP_011536382.1:p.Asp860=
XM_011538081.1:c.2576A=	XP_011536383.1:p.Asp859=
XM_011538082.1:c.2549A=	XP_011536384.1:p.Asp850=
XM_011538080.2:c.2579A=	XP_011536382.1:p.Asp860=
XM_011538081.2:c.2576A=	XP_011536383.1:p.Asp859=
XM_011538082.2:c.2549A=	XP_011536384.1:p.Asp850=
XM_017019090.1:c.2576A=	XP_016874579.1:p.Asp859=
NM_015335.5:c.2579A= MANE Select	NP_056150.1:p.Asp860=