Canonical Allele Identifier: CA2065372103

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982700_115982703delinsAAAG , CM000674.2:g.115982700_115982703delinsAAAG	GRCh38
NC_000012.11:g.116420505_116420508delinsAAAG , CM000674.1:g.116420505_116420508delinsAAAG	GRCh37
NC_000012.10:g.114904888_114904891delinsAAAG	NCBI36
NG_023366.1:g.299484_299487delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-100_4956-97delinsCTTT MANE Select	ENSP00000281928.3:n.4956-100_4956-97delinsCTTT
ENST00000549786.2:c.4384-100_4384-97delinsCTTT
ENST00000648379.1:n.3324-100_3324-97delinsCTTT
ENST00000648737.1:n.4720-100_4720-97delinsCTTT
ENST00000648825.1:n.1696-100_1696-97delinsCTTT
ENST00000648916.1:n.2967-100_2967-97delinsCTTT
ENST00000649146.1:n.2099_2102delinsCTTT
ENST00000649607.1:c.3140-100_3140-97delinsCTTT
ENST00000649775.1:c.1453-108_1453-105delinsCTTT
ENST00000650226.1:c.4956-100_4956-97delinsCTTT	ENSP00000496981.1:n.4956-100_4956-97delinsCTTT
ENST00000281928.7:c.4956-100_4956-97delinsCTTT	ENSP00000281928.3:n.4956-100_4956-97delinsCTTT
ENST00000549786.1:c.320-100_320-97delinsCTTT
NM_015335.4:c.4956-100_4956-97delinsCTTT	NP_056150.1:n.4956-100_4956-97delinsCTTT
XM_011538080.1:c.4956-100_4956-97delinsCTTT	XP_011536382.1:n.4956-100_4956-97delinsCTTT
XM_011538081.1:c.4953-100_4953-97delinsCTTT	XP_011536383.1:n.4953-100_4953-97delinsCTTT
XM_011538082.1:c.4926-100_4926-97delinsCTTT	XP_011536384.1:n.4926-100_4926-97delinsCTTT
XM_011538080.2:c.4956-100_4956-97delinsCTTT	XP_011536382.1:n.4956-100_4956-97delinsCTTT
XM_011538081.2:c.4953-100_4953-97delinsCTTT	XP_011536383.1:n.4953-100_4953-97delinsCTTT
XM_011538082.2:c.4926-100_4926-97delinsCTTT	XP_011536384.1:n.4926-100_4926-97delinsCTTT
XM_017019090.1:c.4953-100_4953-97delinsCTTT	XP_016874579.1:n.4953-100_4953-97delinsCTTT
NM_015335.5:c.4956-100_4956-97delinsCTTT MANE Select	NP_056150.1:n.4956-100_4956-97delinsCTTT