Canonical Allele Identifier: CA2065396798

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997167G= , CM000674.2:g.115997167G=	GRCh38
NC_000012.11:g.116434972G= , CM000674.1:g.116434972G=	GRCh37
NC_000012.10:g.114919355G=	NCBI36
NG_023366.1:g.285020C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.2633C= MANE Select	ENSP00000281928.3:p.Ser878=
ENST00000548743.2:c.2603C=	ENSP00000448553.2:p.Ser868=
ENST00000549786.2:c.2061C=
ENST00000647927.1:n.3006C=
ENST00000648173.1:n.1428C=
ENST00000648379.1:n.1001C=
ENST00000648737.1:n.2397C=
ENST00000648916.1:n.644C=
ENST00000649607.1:c.817C=
ENST00000650226.1:c.2633C=	ENSP00000496981.1:p.Ser878=
ENST00000281928.7:c.2633C=	ENSP00000281928.3:p.Ser878=
NM_015335.4:c.2633C=	NP_056150.1:p.Ser878=
XM_011538080.1:c.2633C=	XP_011536382.1:p.Ser878=
XM_011538081.1:c.2630C=	XP_011536383.1:p.Ser877=
XM_011538082.1:c.2603C=	XP_011536384.1:p.Ser868=
XM_011538080.2:c.2633C=	XP_011536382.1:p.Ser878=
XM_011538081.2:c.2630C=	XP_011536383.1:p.Ser877=
XM_011538082.2:c.2603C=	XP_011536384.1:p.Ser868=
XM_017019090.1:c.2630C=	XP_016874579.1:p.Ser877=
NM_015335.5:c.2633C= MANE Select	NP_056150.1:p.Ser878=