Canonical Allele Identifier: CA2575306506

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982624_115982647del , CM000674.2:g.115982624_115982647del	GRCh38
NC_000012.11:g.116420429_116420452del , CM000674.1:g.116420429_116420452del	GRCh37
NC_000012.10:g.114904812_114904835del	NCBI36
NG_023366.1:g.299541_299564del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.4956-43_4956-20del MANE Select	ENSP00000281928.3:n.4956-43_4956-20del
ENST00000549786.2:c.4384-43_4384-20del
ENST00000648379.1:n.3324-43_3324-20del
ENST00000648737.1:n.4720-43_4720-20del
ENST00000648825.1:n.1696-43_1696-20del
ENST00000648916.1:n.2967-43_2967-20del
ENST00000649146.1:n.2156_2179del
ENST00000649607.1:c.3140-43_3140-20del
ENST00000649775.1:c.1453-51_1453-28del
ENST00000650226.1:c.4956-43_4956-20del	ENSP00000496981.1:n.4956-43_4956-20del
ENST00000281928.7:c.4956-43_4956-20del	ENSP00000281928.3:n.4956-43_4956-20del
ENST00000549786.1:c.320-43_320-20del
NM_015335.4:c.4956-43_4956-20del	NP_056150.1:n.4956-43_4956-20del
XM_011538080.1:c.4956-43_4956-20del	XP_011536382.1:n.4956-43_4956-20del
XM_011538081.1:c.4953-43_4953-20del	XP_011536383.1:n.4953-43_4953-20del
XM_011538082.1:c.4926-43_4926-20del	XP_011536384.1:n.4926-43_4926-20del
XM_011538080.2:c.4956-43_4956-20del	XP_011536382.1:n.4956-43_4956-20del
XM_011538081.2:c.4953-43_4953-20del	XP_011536383.1:n.4953-43_4953-20del
XM_011538082.2:c.4926-43_4926-20del	XP_011536384.1:n.4926-43_4926-20del
XM_017019090.1:c.4953-43_4953-20del	XP_016874579.1:n.4953-43_4953-20del
NM_015335.5:c.4956-43_4956-20del MANE Select	NP_056150.1:n.4956-43_4956-20del