Canonical Allele Identifier: CA2065373199

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115983261G= , CM000674.2:g.115983261G=	GRCh38
NC_000012.11:g.116421066G= , CM000674.1:g.116421066G=	GRCh37
NC_000012.10:g.114905449G=	NCBI36
NG_023366.1:g.298926C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.4811C= MANE Select	ENSP00000281928.3:p.Ser1604=
ENST00000549786.2:c.4239C=
ENST00000648379.1:n.3179C=
ENST00000648737.1:n.4575C=
ENST00000648825.1:n.1551C=
ENST00000648916.1:n.2822C=
ENST00000649146.1:n.1541C=
ENST00000649607.1:c.2995C=
ENST00000649775.1:c.1308C=
ENST00000650226.1:c.4811C=	ENSP00000496981.1:p.Ser1604=
ENST00000281928.7:c.4811C=	ENSP00000281928.3:p.Ser1604=
ENST00000549786.1:c.175C=
NM_015335.4:c.4811C=	NP_056150.1:p.Ser1604=
XM_011538080.1:c.4811C=	XP_011536382.1:p.Ser1604=
XM_011538081.1:c.4808C=	XP_011536383.1:p.Ser1603=
XM_011538082.1:c.4781C=	XP_011536384.1:p.Ser1594=
XM_011538080.2:c.4811C=	XP_011536382.1:p.Ser1604=
XM_011538081.2:c.4808C=	XP_011536383.1:p.Ser1603=
XM_011538082.2:c.4781C=	XP_011536384.1:p.Ser1594=
XM_017019090.1:c.4808C=	XP_016874579.1:p.Ser1603=
NM_015335.5:c.4811C= MANE Select	NP_056150.1:p.Ser1604=