Canonical Allele Identifier: CA2065387172

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991965_115991967delinsAAG , CM000674.2:g.115991965_115991967delinsAAG	GRCh38
NC_000012.11:g.116429770_116429772delinsAAG , CM000674.1:g.116429770_116429772delinsAAG	GRCh37
NC_000012.10:g.114914153_114914155delinsAAG	NCBI36
NG_023366.1:g.290220_290222delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2997-10_2997-8delinsCTT MANE Select	ENSP00000281928.3:n.2997-10_2997-8delinsCTT
ENST00000548743.2:c.2967-10_2967-8delinsCTT	ENSP00000448553.2:n.2967-10_2967-8delinsCTT
ENST00000549786.2:c.2425-10_2425-8delinsCTT
ENST00000648173.1:n.1792-10_1792-8delinsCTT
ENST00000648379.1:n.1365-10_1365-8delinsCTT
ENST00000648737.1:n.2761-10_2761-8delinsCTT
ENST00000648916.1:n.1008-10_1008-8delinsCTT
ENST00000649607.1:c.1181-10_1181-8delinsCTT
ENST00000650226.1:c.2997-10_2997-8delinsCTT	ENSP00000496981.1:n.2997-10_2997-8delinsCTT
ENST00000281928.7:c.2997-10_2997-8delinsCTT	ENSP00000281928.3:n.2997-10_2997-8delinsCTT
NM_015335.4:c.2997-10_2997-8delinsCTT	NP_056150.1:n.2997-10_2997-8delinsCTT
XM_011538080.1:c.2997-10_2997-8delinsCTT	XP_011536382.1:n.2997-10_2997-8delinsCTT
XM_011538081.1:c.2994-10_2994-8delinsCTT	XP_011536383.1:n.2994-10_2994-8delinsCTT
XM_011538082.1:c.2967-10_2967-8delinsCTT	XP_011536384.1:n.2967-10_2967-8delinsCTT
XM_011538080.2:c.2997-10_2997-8delinsCTT	XP_011536382.1:n.2997-10_2997-8delinsCTT
XM_011538081.2:c.2994-10_2994-8delinsCTT	XP_011536383.1:n.2994-10_2994-8delinsCTT
XM_011538082.2:c.2967-10_2967-8delinsCTT	XP_011536384.1:n.2967-10_2967-8delinsCTT
XM_017019090.1:c.2994-10_2994-8delinsCTT	XP_016874579.1:n.2994-10_2994-8delinsCTT
NM_015335.5:c.2997-10_2997-8delinsCTT MANE Select	NP_056150.1:n.2997-10_2997-8delinsCTT