Canonical Allele Identifier: CA2536639448

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997562_115997563insTTAGA , CM000674.2:g.115997562_115997563insTTAGA	GRCh38
NC_000012.11:g.116435367_116435368insTTAGA , CM000674.1:g.116435367_116435368insTTAGA	GRCh37
NC_000012.10:g.114919750_114919751insTTAGA	NCBI36
NG_023366.1:g.284624_284625insTCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2570-333_2570-332insTCTAA MANE Select	ENSP00000281928.3:n.2570-333_2570-332insTCTAA
ENST00000548743.2:c.2540-333_2540-332insTCTAA	ENSP00000448553.2:n.2540-333_2540-332insTCTAA
ENST00000549786.2:c.1998-333_1998-332insTCTAA
ENST00000647927.1:n.2610_2611insTCTAA
ENST00000648173.1:n.1365-333_1365-332insTCTAA
ENST00000648379.1:n.938-333_938-332insTCTAA
ENST00000648737.1:n.2334-333_2334-332insTCTAA
ENST00000648916.1:n.581-333_581-332insTCTAA
ENST00000649607.1:c.757-336_757-335insTCTAA
ENST00000650226.1:c.2570-333_2570-332insTCTAA	ENSP00000496981.1:n.2570-333_2570-332insTCTAA
ENST00000281928.7:c.2570-333_2570-332insTCTAA	ENSP00000281928.3:n.2570-333_2570-332insTCTAA
NM_015335.4:c.2570-333_2570-332insTCTAA	NP_056150.1:n.2570-333_2570-332insTCTAA
XM_011538080.1:c.2570-333_2570-332insTCTAA	XP_011536382.1:n.2570-333_2570-332insTCTAA
XM_011538081.1:c.2570-336_2570-335insTCTAA	XP_011536383.1:n.2570-336_2570-335insTCTAA
XM_011538082.1:c.2540-333_2540-332insTCTAA	XP_011536384.1:n.2540-333_2540-332insTCTAA
XM_011538080.2:c.2570-333_2570-332insTCTAA	XP_011536382.1:n.2570-333_2570-332insTCTAA
XM_011538081.2:c.2570-336_2570-335insTCTAA	XP_011536383.1:n.2570-336_2570-335insTCTAA
XM_011538082.2:c.2540-333_2540-332insTCTAA	XP_011536384.1:n.2540-333_2540-332insTCTAA
XM_017019090.1:c.2570-336_2570-335insTCTAA	XP_016874579.1:n.2570-336_2570-335insTCTAA
NM_015335.5:c.2570-333_2570-332insTCTAA MANE Select	NP_056150.1:n.2570-333_2570-332insTCTAA