Canonical Allele Identifier: CA2065397570

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997587_115997595delinsAATTTTTGT , CM000674.2:g.115997587_115997595delinsAATTTTTGT	GRCh38
NC_000012.11:g.116435392_116435400delinsAATTTTTGT , CM000674.1:g.116435392_116435400delinsAATTTTTGT	GRCh37
NC_000012.10:g.114919775_114919783delinsAATTTTTGT	NCBI36
NG_023366.1:g.284592_284600delinsACAAAAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2570-365_2570-357delinsACAAAAATT MANE Select	ENSP00000281928.3:n.2570-365_2570-357delinsACAAAAATT
ENST00000548743.2:c.2540-365_2540-357delinsACAAAAATT	ENSP00000448553.2:n.2540-365_2540-357delinsACAAAAATT
ENST00000549786.2:c.1998-365_1998-357delinsACAAAAATT
ENST00000647927.1:n.2578_2586delinsACAAAAATT
ENST00000648173.1:n.1365-365_1365-357delinsACAAAAATT
ENST00000648379.1:n.938-365_938-357delinsACAAAAATT
ENST00000648737.1:n.2334-365_2334-357delinsACAAAAATT
ENST00000648916.1:n.581-365_581-357delinsACAAAAATT
ENST00000649607.1:c.757-368_757-360delinsACAAAAATT
ENST00000650226.1:c.2570-365_2570-357delinsACAAAAATT	ENSP00000496981.1:n.2570-365_2570-357delinsACAAAAATT
ENST00000281928.7:c.2570-365_2570-357delinsACAAAAATT	ENSP00000281928.3:n.2570-365_2570-357delinsACAAAAATT
NM_015335.4:c.2570-365_2570-357delinsACAAAAATT	NP_056150.1:n.2570-365_2570-357delinsACAAAAATT
XM_011538080.1:c.2570-365_2570-357delinsACAAAAATT	XP_011536382.1:n.2570-365_2570-357delinsACAAAAATT
XM_011538081.1:c.2570-368_2570-360delinsACAAAAATT	XP_011536383.1:n.2570-368_2570-360delinsACAAAAATT
XM_011538082.1:c.2540-365_2540-357delinsACAAAAATT	XP_011536384.1:n.2540-365_2540-357delinsACAAAAATT
XM_011538080.2:c.2570-365_2570-357delinsACAAAAATT	XP_011536382.1:n.2570-365_2570-357delinsACAAAAATT
XM_011538081.2:c.2570-368_2570-360delinsACAAAAATT	XP_011536383.1:n.2570-368_2570-360delinsACAAAAATT
XM_011538082.2:c.2540-365_2540-357delinsACAAAAATT	XP_011536384.1:n.2540-365_2540-357delinsACAAAAATT
XM_017019090.1:c.2570-368_2570-360delinsACAAAAATT	XP_016874579.1:n.2570-368_2570-360delinsACAAAAATT
NM_015335.5:c.2570-365_2570-357delinsACAAAAATT MANE Select	NP_056150.1:n.2570-365_2570-357delinsACAAAAATT