Canonical Allele Identifier: CA2516911149

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970794_115970795insGC , CM000674.2:g.115970794_115970795insGC	GRCh38
NC_000012.11:g.116408599_116408600insGC , CM000674.1:g.116408599_116408600insGC	GRCh37
NC_000012.10:g.114892982_114892983insGC	NCBI36
NG_023366.1:g.311392_311393insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5891-25_5891-24insGC MANE Select	ENSP00000281928.3:n.5891-25_5891-24insGC
ENST00000548694.2:n.881-25_881-24insGC
ENST00000548784.2:n.2105-25_2105-24insGC
ENST00000648379.1:n.4259-25_4259-24insGC
ENST00000648737.1:n.5655-25_5655-24insGC
ENST00000648825.1:n.4076-25_4076-24insGC
ENST00000648916.1:n.3902-25_3902-24insGC
ENST00000649607.1:c.4075-25_4075-24insGC
ENST00000649775.1:c.2380-25_2380-24insGC
ENST00000650226.1:c.5927-25_5927-24insGC	ENSP00000496981.1:n.5927-25_5927-24insGC
ENST00000281928.7:c.5891-25_5891-24insGC	ENSP00000281928.3:n.5891-25_5891-24insGC
ENST00000548784.1:n.389-25_389-24insGC
ENST00000552447.1:c.504-25_504-24insGC
NM_015335.4:c.5891-25_5891-24insGC	NP_056150.1:n.5891-25_5891-24insGC
XM_011538080.1:c.5927-25_5927-24insGC	XP_011536382.1:n.5927-25_5927-24insGC
XM_011538081.1:c.5924-25_5924-24insGC	XP_011536383.1:n.5924-25_5924-24insGC
XM_011538082.1:c.5897-25_5897-24insGC	XP_011536384.1:n.5897-25_5897-24insGC
XM_011538080.2:c.5927-25_5927-24insGC	XP_011536382.1:n.5927-25_5927-24insGC
XM_011538081.2:c.5924-25_5924-24insGC	XP_011536383.1:n.5924-25_5924-24insGC
XM_011538082.2:c.5897-25_5897-24insGC	XP_011536384.1:n.5897-25_5897-24insGC
XM_017019090.1:c.5888-25_5888-24insGC	XP_016874579.1:n.5888-25_5888-24insGC
NM_015335.5:c.5891-25_5891-24insGC MANE Select	NP_056150.1:n.5891-25_5891-24insGC