Canonical Allele Identifier: CA2065375748

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984412_115984413delinsAT , CM000674.2:g.115984412_115984413delinsAT	GRCh38
NC_000012.11:g.116422217_116422218delinsAT , CM000674.1:g.116422217_116422218delinsAT	GRCh37
NC_000012.10:g.114906600_114906601delinsAT	NCBI36
NG_023366.1:g.297774_297775delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-41_4339-40delinsAT MANE Select	ENSP00000281928.3:n.4339-41_4339-40delinsAT
ENST00000549786.2:c.3767-41_3767-40delinsAT
ENST00000648379.1:n.2707-41_2707-40delinsAT
ENST00000648737.1:n.4103-41_4103-40delinsAT
ENST00000648825.1:n.1079-41_1079-40delinsAT
ENST00000648916.1:n.2350-41_2350-40delinsAT
ENST00000649146.1:n.1028_1029delinsAT
ENST00000649607.1:c.2523-41_2523-40delinsAT
ENST00000649775.1:c.836-41_836-40delinsAT
ENST00000650091.1:n.2315-41_2315-40delinsAT
ENST00000650226.1:c.4339-41_4339-40delinsAT	ENSP00000496981.1:n.4339-41_4339-40delinsAT
ENST00000281928.7:c.4339-41_4339-40delinsAT	ENSP00000281928.3:n.4339-41_4339-40delinsAT
NM_015335.4:c.4339-41_4339-40delinsAT	NP_056150.1:n.4339-41_4339-40delinsAT
XM_011538080.1:c.4339-41_4339-40delinsAT	XP_011536382.1:n.4339-41_4339-40delinsAT
XM_011538081.1:c.4336-41_4336-40delinsAT	XP_011536383.1:n.4336-41_4336-40delinsAT
XM_011538082.1:c.4309-41_4309-40delinsAT	XP_011536384.1:n.4309-41_4309-40delinsAT
XM_011538080.2:c.4339-41_4339-40delinsAT	XP_011536382.1:n.4339-41_4339-40delinsAT
XM_011538081.2:c.4336-41_4336-40delinsAT	XP_011536383.1:n.4336-41_4336-40delinsAT
XM_011538082.2:c.4309-41_4309-40delinsAT	XP_011536384.1:n.4309-41_4309-40delinsAT
XM_017019090.1:c.4336-41_4336-40delinsAT	XP_016874579.1:n.4336-41_4336-40delinsAT
NM_015335.5:c.4339-41_4339-40delinsAT MANE Select	NP_056150.1:n.4339-41_4339-40delinsAT