Canonical Allele Identifier: CA2065395865

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996671T= , CM000674.2:g.115996671T=	GRCh38
NC_000012.11:g.116434476T= , CM000674.1:g.116434476T=	GRCh37
NC_000012.10:g.114918859T=	NCBI36
NG_023366.1:g.285516A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2801A= MANE Select	ENSP00000281928.3:p.Tyr934=
ENST00000548743.2:c.2771A=	ENSP00000448553.2:p.Tyr924=
ENST00000549786.2:c.2229A=
ENST00000647927.1:n.3174A=
ENST00000648173.1:n.1596A=
ENST00000648379.1:n.1169A=
ENST00000648737.1:n.2565A=
ENST00000648916.1:n.812A=
ENST00000649607.1:c.985A=
ENST00000650226.1:c.2801A=	ENSP00000496981.1:p.Tyr934=
ENST00000281928.7:c.2801A=	ENSP00000281928.3:p.Tyr934=
NM_015335.4:c.2801A=	NP_056150.1:p.Tyr934=
XM_011538080.1:c.2801A=	XP_011536382.1:p.Tyr934=
XM_011538081.1:c.2798A=	XP_011536383.1:p.Tyr933=
XM_011538082.1:c.2771A=	XP_011536384.1:p.Tyr924=
XM_011538080.2:c.2801A=	XP_011536382.1:p.Tyr934=
XM_011538081.2:c.2798A=	XP_011536383.1:p.Tyr933=
XM_011538082.2:c.2771A=	XP_011536384.1:p.Tyr924=
XM_017019090.1:c.2798A=	XP_016874579.1:p.Tyr933=
NM_015335.5:c.2801A= MANE Select	NP_056150.1:p.Tyr934=