Canonical Allele Identifier: CA2065372029

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982673_115982674delinsCT , CM000674.2:g.115982673_115982674delinsCT	GRCh38
NC_000012.11:g.116420478_116420479delinsCT , CM000674.1:g.116420478_116420479delinsCT	GRCh37
NC_000012.10:g.114904861_114904862delinsCT	NCBI36
NG_023366.1:g.299513_299514delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-71_4956-70delinsAG MANE Select	ENSP00000281928.3:n.4956-71_4956-70delinsAG
ENST00000549786.2:c.4384-71_4384-70delinsAG
ENST00000648379.1:n.3324-71_3324-70delinsAG
ENST00000648737.1:n.4720-71_4720-70delinsAG
ENST00000648825.1:n.1696-71_1696-70delinsAG
ENST00000648916.1:n.2967-71_2967-70delinsAG
ENST00000649146.1:n.2128_2129delinsAG
ENST00000649607.1:c.3140-71_3140-70delinsAG
ENST00000649775.1:c.1453-79_1453-78delinsAG
ENST00000650226.1:c.4956-71_4956-70delinsAG	ENSP00000496981.1:n.4956-71_4956-70delinsAG
ENST00000281928.7:c.4956-71_4956-70delinsAG	ENSP00000281928.3:n.4956-71_4956-70delinsAG
ENST00000549786.1:c.320-71_320-70delinsAG
NM_015335.4:c.4956-71_4956-70delinsAG	NP_056150.1:n.4956-71_4956-70delinsAG
XM_011538080.1:c.4956-71_4956-70delinsAG	XP_011536382.1:n.4956-71_4956-70delinsAG
XM_011538081.1:c.4953-71_4953-70delinsAG	XP_011536383.1:n.4953-71_4953-70delinsAG
XM_011538082.1:c.4926-71_4926-70delinsAG	XP_011536384.1:n.4926-71_4926-70delinsAG
XM_011538080.2:c.4956-71_4956-70delinsAG	XP_011536382.1:n.4956-71_4956-70delinsAG
XM_011538081.2:c.4953-71_4953-70delinsAG	XP_011536383.1:n.4953-71_4953-70delinsAG
XM_011538082.2:c.4926-71_4926-70delinsAG	XP_011536384.1:n.4926-71_4926-70delinsAG
XM_017019090.1:c.4953-71_4953-70delinsAG	XP_016874579.1:n.4953-71_4953-70delinsAG
NM_015335.5:c.4956-71_4956-70delinsAG MANE Select	NP_056150.1:n.4956-71_4956-70delinsAG