Canonical Allele Identifier: CA2065397598

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997610_115997611delinsCA , CM000674.2:g.115997610_115997611delinsCA	GRCh38
NC_000012.11:g.116435415_116435416delinsCA , CM000674.1:g.116435415_116435416delinsCA	GRCh37
NC_000012.10:g.114919798_114919799delinsCA	NCBI36
NG_023366.1:g.284576_284577delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2570-381_2570-380delinsTG MANE Select	ENSP00000281928.3:n.2570-381_2570-380delinsTG
ENST00000548743.2:c.2540-381_2540-380delinsTG	ENSP00000448553.2:n.2540-381_2540-380delinsTG
ENST00000549786.2:c.1998-381_1998-380delinsTG
ENST00000647927.1:n.2562_2563delinsTG
ENST00000648173.1:n.1365-381_1365-380delinsTG
ENST00000648379.1:n.938-381_938-380delinsTG
ENST00000648737.1:n.2334-381_2334-380delinsTG
ENST00000648916.1:n.581-381_581-380delinsTG
ENST00000649607.1:c.757-384_757-383delinsTG
ENST00000650226.1:c.2570-381_2570-380delinsTG	ENSP00000496981.1:n.2570-381_2570-380delinsTG
ENST00000281928.7:c.2570-381_2570-380delinsTG	ENSP00000281928.3:n.2570-381_2570-380delinsTG
NM_015335.4:c.2570-381_2570-380delinsTG	NP_056150.1:n.2570-381_2570-380delinsTG
XM_011538080.1:c.2570-381_2570-380delinsTG	XP_011536382.1:n.2570-381_2570-380delinsTG
XM_011538081.1:c.2570-384_2570-383delinsTG	XP_011536383.1:n.2570-384_2570-383delinsTG
XM_011538082.1:c.2540-381_2540-380delinsTG	XP_011536384.1:n.2540-381_2540-380delinsTG
XM_011538080.2:c.2570-381_2570-380delinsTG	XP_011536382.1:n.2570-381_2570-380delinsTG
XM_011538081.2:c.2570-384_2570-383delinsTG	XP_011536383.1:n.2570-384_2570-383delinsTG
XM_011538082.2:c.2540-381_2540-380delinsTG	XP_011536384.1:n.2540-381_2540-380delinsTG
XM_017019090.1:c.2570-384_2570-383delinsTG	XP_016874579.1:n.2570-384_2570-383delinsTG
NM_015335.5:c.2570-381_2570-380delinsTG MANE Select	NP_056150.1:n.2570-381_2570-380delinsTG