Canonical Allele Identifier: CA2065371883

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982606_115982608delinsGGA , CM000674.2:g.115982606_115982608delinsGGA	GRCh38
NC_000012.11:g.116420411_116420413delinsGGA , CM000674.1:g.116420411_116420413delinsGGA	GRCh37
NC_000012.10:g.114904794_114904796delinsGGA	NCBI36
NG_023366.1:g.299579_299581delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-5_4956-3delinsTCC MANE Select	ENSP00000281928.3:n.4956-5_4956-3delinsTCC
ENST00000549786.2:c.4384-5_4384-3delinsTCC
ENST00000648379.1:n.3324-5_3324-3delinsTCC
ENST00000648737.1:n.4720-5_4720-3delinsTCC
ENST00000648825.1:n.1696-5_1696-3delinsTCC
ENST00000648916.1:n.2967-5_2967-3delinsTCC
ENST00000649146.1:n.2194_2196delinsTCC
ENST00000649607.1:c.3140-5_3140-3delinsTCC
ENST00000649775.1:c.1453-13_1453-11delinsTCC
ENST00000650226.1:c.4956-5_4956-3delinsTCC	ENSP00000496981.1:n.4956-5_4956-3delinsTCC
ENST00000281928.7:c.4956-5_4956-3delinsTCC	ENSP00000281928.3:n.4956-5_4956-3delinsTCC
ENST00000549786.1:c.320-5_320-3delinsTCC
NM_015335.4:c.4956-5_4956-3delinsTCC	NP_056150.1:n.4956-5_4956-3delinsTCC
XM_011538080.1:c.4956-5_4956-3delinsTCC	XP_011536382.1:n.4956-5_4956-3delinsTCC
XM_011538081.1:c.4953-5_4953-3delinsTCC	XP_011536383.1:n.4953-5_4953-3delinsTCC
XM_011538082.1:c.4926-5_4926-3delinsTCC	XP_011536384.1:n.4926-5_4926-3delinsTCC
XM_011538080.2:c.4956-5_4956-3delinsTCC	XP_011536382.1:n.4956-5_4956-3delinsTCC
XM_011538081.2:c.4953-5_4953-3delinsTCC	XP_011536383.1:n.4953-5_4953-3delinsTCC
XM_011538082.2:c.4926-5_4926-3delinsTCC	XP_011536384.1:n.4926-5_4926-3delinsTCC
XM_017019090.1:c.4953-5_4953-3delinsTCC	XP_016874579.1:n.4953-5_4953-3delinsTCC
NM_015335.5:c.4956-5_4956-3delinsTCC MANE Select	NP_056150.1:n.4956-5_4956-3delinsTCC