Canonical Allele Identifier: CA2065375747

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984412_115984416delinsATTCC , CM000674.2:g.115984412_115984416delinsATTCC	GRCh38
NC_000012.11:g.116422217_116422221delinsATTCC , CM000674.1:g.116422217_116422221delinsATTCC	GRCh37
NC_000012.10:g.114906600_114906604delinsATTCC	NCBI36
NG_023366.1:g.297771_297775delinsGGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-44_4339-40delinsGGAAT MANE Select	ENSP00000281928.3:n.4339-44_4339-40delinsGGAAT
ENST00000549786.2:c.3767-44_3767-40delinsGGAAT
ENST00000648379.1:n.2707-44_2707-40delinsGGAAT
ENST00000648737.1:n.4103-44_4103-40delinsGGAAT
ENST00000648825.1:n.1079-44_1079-40delinsGGAAT
ENST00000648916.1:n.2350-44_2350-40delinsGGAAT
ENST00000649146.1:n.1025_1029delinsGGAAT
ENST00000649607.1:c.2523-44_2523-40delinsGGAAT
ENST00000649775.1:c.836-44_836-40delinsGGAAT
ENST00000650091.1:n.2315-44_2315-40delinsGGAAT
ENST00000650226.1:c.4339-44_4339-40delinsGGAAT	ENSP00000496981.1:n.4339-44_4339-40delinsGGAAT
ENST00000281928.7:c.4339-44_4339-40delinsGGAAT	ENSP00000281928.3:n.4339-44_4339-40delinsGGAAT
NM_015335.4:c.4339-44_4339-40delinsGGAAT	NP_056150.1:n.4339-44_4339-40delinsGGAAT
XM_011538080.1:c.4339-44_4339-40delinsGGAAT	XP_011536382.1:n.4339-44_4339-40delinsGGAAT
XM_011538081.1:c.4336-44_4336-40delinsGGAAT	XP_011536383.1:n.4336-44_4336-40delinsGGAAT
XM_011538082.1:c.4309-44_4309-40delinsGGAAT	XP_011536384.1:n.4309-44_4309-40delinsGGAAT
XM_011538080.2:c.4339-44_4339-40delinsGGAAT	XP_011536382.1:n.4339-44_4339-40delinsGGAAT
XM_011538081.2:c.4336-44_4336-40delinsGGAAT	XP_011536383.1:n.4336-44_4336-40delinsGGAAT
XM_011538082.2:c.4309-44_4309-40delinsGGAAT	XP_011536384.1:n.4309-44_4309-40delinsGGAAT
XM_017019090.1:c.4336-44_4336-40delinsGGAAT	XP_016874579.1:n.4336-44_4336-40delinsGGAAT
NM_015335.5:c.4339-44_4339-40delinsGGAAT MANE Select	NP_056150.1:n.4339-44_4339-40delinsGGAAT