Canonical Allele Identifier: CA2065359682

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975526A= , CM000674.2:g.115975526A=	GRCh38
NC_000012.11:g.116413331A= , CM000674.1:g.116413331A=	GRCh37
NC_000012.10:g.114897714A=	NCBI36
NG_023366.1:g.306661T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5577T= MANE Select	ENSP00000281928.3:p.Ala1859=
ENST00000548694.2:n.366T=
ENST00000648379.1:n.3945T=
ENST00000648737.1:n.5341T=
ENST00000648825.1:n.3762T=
ENST00000648916.1:n.3588T=
ENST00000649607.1:c.3761T=
ENST00000649775.1:c.2066T=
ENST00000650226.1:c.5577T=	ENSP00000496981.1:p.Ala1859=
ENST00000281928.7:c.5577T=	ENSP00000281928.3:p.Ala1859=
ENST00000548694.1:n.366T=
ENST00000552447.1:c.154T=
NM_015335.4:c.5577T=	NP_056150.1:p.Ala1859=
XM_011538080.1:c.5577T=	XP_011536382.1:p.Ala1859=
XM_011538081.1:c.5574T=	XP_011536383.1:p.Ala1858=
XM_011538082.1:c.5547T=	XP_011536384.1:p.Ala1849=
XM_011538080.2:c.5577T=	XP_011536382.1:p.Ala1859=
XM_011538081.2:c.5574T=	XP_011536383.1:p.Ala1858=
XM_011538082.2:c.5547T=	XP_011536384.1:p.Ala1849=
XM_017019090.1:c.5574T=	XP_016874579.1:p.Ala1858=
NM_015335.5:c.5577T= MANE Select	NP_056150.1:p.Ala1859=