Canonical Allele Identifier: CA2065410910

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970686G= , CM000674.2:g.115970686G=	GRCh38
NC_000012.11:g.116408491G= , CM000674.1:g.116408491G=	GRCh37
NC_000012.10:g.114892874G=	NCBI36
NG_023366.1:g.311501C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5975C= MANE Select	ENSP00000281928.3:p.Ser1992=
ENST00000548784.2:n.2189C=
ENST00000648379.1:n.4343C=
ENST00000648737.1:n.5739C=
ENST00000648825.1:n.4160C=
ENST00000648916.1:n.3986C=
ENST00000649607.1:c.4159C=
ENST00000649775.1:c.2464C=
ENST00000650226.1:c.6011C=	ENSP00000496981.1:p.Ser2004=
ENST00000281928.7:c.5975C=	ENSP00000281928.3:p.Ser1992=
ENST00000548784.1:n.473C=
NM_015335.4:c.5975C=	NP_056150.1:p.Ser1992=
XM_011538080.1:c.6011C=	XP_011536382.1:p.Ser2004=
XM_011538081.1:c.6008C=	XP_011536383.1:p.Ser2003=
XM_011538082.1:c.5981C=	XP_011536384.1:p.Ser1994=
XM_011538080.2:c.6011C=	XP_011536382.1:p.Ser2004=
XM_011538081.2:c.6008C=	XP_011536383.1:p.Ser2003=
XM_011538082.2:c.5981C=	XP_011536384.1:p.Ser1994=
XM_017019090.1:c.5972C=	XP_016874579.1:p.Ser1991=
NM_015335.5:c.5975C= MANE Select	NP_056150.1:p.Ser1992=