Canonical Allele Identifier: CA2065412965

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975375_115975376delinsCT , CM000674.2:g.115975375_115975376delinsCT	GRCh38
NC_000012.11:g.116413180_116413181delinsCT , CM000674.1:g.116413180_116413181delinsCT	GRCh37
NC_000012.10:g.114897563_114897564delinsCT	NCBI36
NG_023366.1:g.306811_306812delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-63_5589-62delinsAG MANE Select	ENSP00000281928.3:n.5589-63_5589-62delinsAG
ENST00000548694.2:n.516_517delinsAG
ENST00000648379.1:n.3957-63_3957-62delinsAG
ENST00000648737.1:n.5353-63_5353-62delinsAG
ENST00000648825.1:n.3774-63_3774-62delinsAG
ENST00000648916.1:n.3600-63_3600-62delinsAG
ENST00000649607.1:c.3773-63_3773-62delinsAG
ENST00000649775.1:c.2078-63_2078-62delinsAG
ENST00000650226.1:c.5589-27_5589-26delinsAG	ENSP00000496981.1:n.5589-27_5589-26delinsAG
ENST00000281928.7:c.5589-63_5589-62delinsAG	ENSP00000281928.3:n.5589-63_5589-62delinsAG
ENST00000548694.1:n.516_517delinsAG
ENST00000552447.1:c.166-27_166-26delinsAG
NM_015335.4:c.5589-63_5589-62delinsAG	NP_056150.1:n.5589-63_5589-62delinsAG
XM_011538080.1:c.5589-27_5589-26delinsAG	XP_011536382.1:n.5589-27_5589-26delinsAG
XM_011538081.1:c.5586-27_5586-26delinsAG	XP_011536383.1:n.5586-27_5586-26delinsAG
XM_011538082.1:c.5559-27_5559-26delinsAG	XP_011536384.1:n.5559-27_5559-26delinsAG
XM_011538080.2:c.5589-27_5589-26delinsAG	XP_011536382.1:n.5589-27_5589-26delinsAG
XM_011538081.2:c.5586-27_5586-26delinsAG	XP_011536383.1:n.5586-27_5586-26delinsAG
XM_011538082.2:c.5559-27_5559-26delinsAG	XP_011536384.1:n.5559-27_5559-26delinsAG
XM_017019090.1:c.5586-63_5586-62delinsAG	XP_016874579.1:n.5586-63_5586-62delinsAG
NM_015335.5:c.5589-63_5589-62delinsAG MANE Select	NP_056150.1:n.5589-63_5589-62delinsAG