Canonical Allele Identifier: CA2065372096

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982698_115982699delinsCT , CM000674.2:g.115982698_115982699delinsCT	GRCh38
NC_000012.11:g.116420503_116420504delinsCT , CM000674.1:g.116420503_116420504delinsCT	GRCh37
NC_000012.10:g.114904886_114904887delinsCT	NCBI36
NG_023366.1:g.299488_299489delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-96_4956-95delinsAG MANE Select	ENSP00000281928.3:n.4956-96_4956-95delinsAG
ENST00000549786.2:c.4384-96_4384-95delinsAG
ENST00000648379.1:n.3324-96_3324-95delinsAG
ENST00000648737.1:n.4720-96_4720-95delinsAG
ENST00000648825.1:n.1696-96_1696-95delinsAG
ENST00000648916.1:n.2967-96_2967-95delinsAG
ENST00000649146.1:n.2103_2104delinsAG
ENST00000649607.1:c.3140-96_3140-95delinsAG
ENST00000649775.1:c.1453-104_1453-103delinsAG
ENST00000650226.1:c.4956-96_4956-95delinsAG	ENSP00000496981.1:n.4956-96_4956-95delinsAG
ENST00000281928.7:c.4956-96_4956-95delinsAG	ENSP00000281928.3:n.4956-96_4956-95delinsAG
ENST00000549786.1:c.320-96_320-95delinsAG
NM_015335.4:c.4956-96_4956-95delinsAG	NP_056150.1:n.4956-96_4956-95delinsAG
XM_011538080.1:c.4956-96_4956-95delinsAG	XP_011536382.1:n.4956-96_4956-95delinsAG
XM_011538081.1:c.4953-96_4953-95delinsAG	XP_011536383.1:n.4953-96_4953-95delinsAG
XM_011538082.1:c.4926-96_4926-95delinsAG	XP_011536384.1:n.4926-96_4926-95delinsAG
XM_011538080.2:c.4956-96_4956-95delinsAG	XP_011536382.1:n.4956-96_4956-95delinsAG
XM_011538081.2:c.4953-96_4953-95delinsAG	XP_011536383.1:n.4953-96_4953-95delinsAG
XM_011538082.2:c.4926-96_4926-95delinsAG	XP_011536384.1:n.4926-96_4926-95delinsAG
XM_017019090.1:c.4953-96_4953-95delinsAG	XP_016874579.1:n.4953-96_4953-95delinsAG
NM_015335.5:c.4956-96_4956-95delinsAG MANE Select	NP_056150.1:n.4956-96_4956-95delinsAG