Canonical Allele Identifier: CA2065396079

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996782_115996783delinsAT , CM000674.2:g.115996782_115996783delinsAT	GRCh38
NC_000012.11:g.116434587_116434588delinsAT , CM000674.1:g.116434587_116434588delinsAT	GRCh37
NC_000012.10:g.114918970_114918971delinsAT	NCBI36
NG_023366.1:g.285404_285405delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-102_2791-101delinsAT MANE Select	ENSP00000281928.3:n.2791-102_2791-101delinsAT
ENST00000548743.2:c.2761-102_2761-101delinsAT	ENSP00000448553.2:n.2761-102_2761-101delinsAT
ENST00000549786.2:c.2219-102_2219-101delinsAT
ENST00000647927.1:n.3164-102_3164-101delinsAT
ENST00000648173.1:n.1586-102_1586-101delinsAT
ENST00000648379.1:n.1159-102_1159-101delinsAT
ENST00000648737.1:n.2555-102_2555-101delinsAT
ENST00000648916.1:n.802-102_802-101delinsAT
ENST00000649607.1:c.975-102_975-101delinsAT
ENST00000650226.1:c.2791-102_2791-101delinsAT	ENSP00000496981.1:n.2791-102_2791-101delinsAT
ENST00000281928.7:c.2791-102_2791-101delinsAT	ENSP00000281928.3:n.2791-102_2791-101delinsAT
NM_015335.4:c.2791-102_2791-101delinsAT	NP_056150.1:n.2791-102_2791-101delinsAT
XM_011538080.1:c.2791-102_2791-101delinsAT	XP_011536382.1:n.2791-102_2791-101delinsAT
XM_011538081.1:c.2788-102_2788-101delinsAT	XP_011536383.1:n.2788-102_2788-101delinsAT
XM_011538082.1:c.2761-102_2761-101delinsAT	XP_011536384.1:n.2761-102_2761-101delinsAT
XM_011538080.2:c.2791-102_2791-101delinsAT	XP_011536382.1:n.2791-102_2791-101delinsAT
XM_011538081.2:c.2788-102_2788-101delinsAT	XP_011536383.1:n.2788-102_2788-101delinsAT
XM_011538082.2:c.2761-102_2761-101delinsAT	XP_011536384.1:n.2761-102_2761-101delinsAT
XM_017019090.1:c.2788-102_2788-101delinsAT	XP_016874579.1:n.2788-102_2788-101delinsAT
NM_015335.5:c.2791-102_2791-101delinsAT MANE Select	NP_056150.1:n.2791-102_2791-101delinsAT