Canonical Allele Identifier: CA2065410937

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970771_115970772delinsCT , CM000674.2:g.115970771_115970772delinsCT	GRCh38
NC_000012.11:g.116408576_116408577delinsCT , CM000674.1:g.116408576_116408577delinsCT	GRCh37
NC_000012.10:g.114892959_114892960delinsCT	NCBI36
NG_023366.1:g.311415_311416delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5891-2_5891-1delinsAG MANE Select	ENSP00000281928.3:n.5891-2_5891-1delinsAG
ENST00000548694.2:n.881-2_881-1delinsAG
ENST00000548784.2:n.2105-2_2105-1delinsAG
ENST00000648379.1:n.4259-2_4259-1delinsAG
ENST00000648737.1:n.5655-2_5655-1delinsAG
ENST00000648825.1:n.4076-2_4076-1delinsAG
ENST00000648916.1:n.3902-2_3902-1delinsAG
ENST00000649607.1:c.4075-2_4075-1delinsAG
ENST00000649775.1:c.2380-2_2380-1delinsAG
ENST00000650226.1:c.5927-2_5927-1delinsAG	ENSP00000496981.1:n.5927-2_5927-1delinsAG
ENST00000281928.7:c.5891-2_5891-1delinsAG	ENSP00000281928.3:n.5891-2_5891-1delinsAG
ENST00000548784.1:n.389-2_389-1delinsAG
ENST00000552447.1:c.504-2_504-1delinsAG
NM_015335.4:c.5891-2_5891-1delinsAG	NP_056150.1:n.5891-2_5891-1delinsAG
XM_011538080.1:c.5927-2_5927-1delinsAG	XP_011536382.1:n.5927-2_5927-1delinsAG
XM_011538081.1:c.5924-2_5924-1delinsAG	XP_011536383.1:n.5924-2_5924-1delinsAG
XM_011538082.1:c.5897-2_5897-1delinsAG	XP_011536384.1:n.5897-2_5897-1delinsAG
XM_011538080.2:c.5927-2_5927-1delinsAG	XP_011536382.1:n.5927-2_5927-1delinsAG
XM_011538081.2:c.5924-2_5924-1delinsAG	XP_011536383.1:n.5924-2_5924-1delinsAG
XM_011538082.2:c.5897-2_5897-1delinsAG	XP_011536384.1:n.5897-2_5897-1delinsAG
XM_017019090.1:c.5888-2_5888-1delinsAG	XP_016874579.1:n.5888-2_5888-1delinsAG
NM_015335.5:c.5891-2_5891-1delinsAG MANE Select	NP_056150.1:n.5891-2_5891-1delinsAG