Canonical Allele Identifier: CA2741291149

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982620_115982621dup , CM000674.2:g.115982620_115982621dup	GRCh38
NC_000012.11:g.116420425_116420426dup , CM000674.1:g.116420425_116420426dup	GRCh37
NC_000012.10:g.114904808_114904809dup	NCBI36
NG_023366.1:g.299566_299567dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-18_4956-17dup MANE Select	ENSP00000281928.3:n.4956-18_4956-17dup
ENST00000549786.2:c.4384-18_4384-17dup
ENST00000648379.1:n.3324-18_3324-17dup
ENST00000648737.1:n.4720-18_4720-17dup
ENST00000648825.1:n.1696-18_1696-17dup
ENST00000648916.1:n.2967-18_2967-17dup
ENST00000649146.1:n.2181_2182dup
ENST00000649607.1:c.3140-18_3140-17dup
ENST00000649775.1:c.1453-26_1453-25dup
ENST00000650226.1:c.4956-18_4956-17dup	ENSP00000496981.1:n.4956-18_4956-17dup
ENST00000281928.7:c.4956-18_4956-17dup	ENSP00000281928.3:n.4956-18_4956-17dup
ENST00000549786.1:c.320-18_320-17dup
NM_015335.4:c.4956-18_4956-17dup	NP_056150.1:n.4956-18_4956-17dup
XM_011538080.1:c.4956-18_4956-17dup	XP_011536382.1:n.4956-18_4956-17dup
XM_011538081.1:c.4953-18_4953-17dup	XP_011536383.1:n.4953-18_4953-17dup
XM_011538082.1:c.4926-18_4926-17dup	XP_011536384.1:n.4926-18_4926-17dup
XM_011538080.2:c.4956-18_4956-17dup	XP_011536382.1:n.4956-18_4956-17dup
XM_011538081.2:c.4953-18_4953-17dup	XP_011536383.1:n.4953-18_4953-17dup
XM_011538082.2:c.4926-18_4926-17dup	XP_011536384.1:n.4926-18_4926-17dup
XM_017019090.1:c.4953-18_4953-17dup	XP_016874579.1:n.4953-18_4953-17dup
NM_015335.5:c.4956-18_4956-17dup MANE Select	NP_056150.1:n.4956-18_4956-17dup