Canonical Allele Identifier: CA2065372168

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982772G= , CM000674.2:g.115982772G=	GRCh38
NC_000012.11:g.116420577G= , CM000674.1:g.116420577G=	GRCh37
NC_000012.10:g.114904960G=	NCBI36
NG_023366.1:g.299415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-169C= MANE Select	ENSP00000281928.3:n.4956-169C=
ENST00000549786.2:c.4384-169C=
ENST00000648379.1:n.3324-169C=
ENST00000648737.1:n.4720-169C=
ENST00000648825.1:n.1696-169C=
ENST00000648916.1:n.2967-169C=
ENST00000649146.1:n.2030C=
ENST00000649607.1:c.3140-169C=
ENST00000649775.1:c.1453-177C=
ENST00000650226.1:c.4956-169C=	ENSP00000496981.1:n.4956-169C=
ENST00000281928.7:c.4956-169C=	ENSP00000281928.3:n.4956-169C=
ENST00000549786.1:c.320-169C=
NM_015335.4:c.4956-169C=	NP_056150.1:n.4956-169C=
XM_011538080.1:c.4956-169C=	XP_011536382.1:n.4956-169C=
XM_011538081.1:c.4953-169C=	XP_011536383.1:n.4953-169C=
XM_011538082.1:c.4926-169C=	XP_011536384.1:n.4926-169C=
XM_011538080.2:c.4956-169C=	XP_011536382.1:n.4956-169C=
XM_011538081.2:c.4953-169C=	XP_011536383.1:n.4953-169C=
XM_011538082.2:c.4926-169C=	XP_011536384.1:n.4926-169C=
XM_017019090.1:c.4953-169C=	XP_016874579.1:n.4953-169C=
NM_015335.5:c.4956-169C= MANE Select	NP_056150.1:n.4956-169C=