Canonical Allele Identifier: CA2520986134

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116003172_116003173insT , CM000674.2:g.116003172_116003173insT	GRCh38
NC_000012.11:g.116440977_116440978insT , CM000674.1:g.116440977_116440978insT	GRCh37
NC_000012.10:g.114925360_114925361insT	NCBI36
NG_023366.1:g.279014_279015insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2470-71_2470-70insA MANE Select	ENSP00000281928.3:n.2470-71_2470-70insA
ENST00000548743.2:c.2440-71_2440-70insA	ENSP00000448553.2:n.2440-71_2440-70insA
ENST00000549786.2:c.1898-71_1898-70insA
ENST00000648173.1:n.1265-71_1265-70insA
ENST00000648379.1:n.767_768insA
ENST00000648737.1:n.2234-71_2234-70insA
ENST00000648916.1:n.481-71_481-70insA
ENST00000649607.1:c.657-71_657-70insA
ENST00000650226.1:c.2470-71_2470-70insA	ENSP00000496981.1:n.2470-71_2470-70insA
ENST00000281928.7:c.2470-71_2470-70insA	ENSP00000281928.3:n.2470-71_2470-70insA
NM_015335.4:c.2470-71_2470-70insA	NP_056150.1:n.2470-71_2470-70insA
XM_011538080.1:c.2470-71_2470-70insA	XP_011536382.1:n.2470-71_2470-70insA
XM_011538081.1:c.2470-71_2470-70insA	XP_011536383.1:n.2470-71_2470-70insA
XM_011538082.1:c.2440-71_2440-70insA	XP_011536384.1:n.2440-71_2440-70insA
XM_011538080.2:c.2470-71_2470-70insA	XP_011536382.1:n.2470-71_2470-70insA
XM_011538081.2:c.2470-71_2470-70insA	XP_011536383.1:n.2470-71_2470-70insA
XM_011538082.2:c.2440-71_2440-70insA	XP_011536384.1:n.2440-71_2440-70insA
XM_017019090.1:c.2470-71_2470-70insA	XP_016874579.1:n.2470-71_2470-70insA
NM_015335.5:c.2470-71_2470-70insA MANE Select	NP_056150.1:n.2470-71_2470-70insA