Canonical Allele Identifier: CA2621141608

Gene: MED13L

Linked Data

• gnomAD v4: 12-115982675-C-CTAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982675_115982676insTAG , CM000674.2:g.115982675_115982676insTAG	GRCh38
NC_000012.11:g.116420480_116420481insTAG , CM000674.1:g.116420480_116420481insTAG	GRCh37
NC_000012.10:g.114904863_114904864insTAG	NCBI36
NG_023366.1:g.299511_299512insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-73_4956-72insCTA MANE Select	ENSP00000281928.3:n.4956-73_4956-72insCTA
ENST00000549786.2:c.4384-73_4384-72insCTA
ENST00000648379.1:n.3324-73_3324-72insCTA
ENST00000648737.1:n.4720-73_4720-72insCTA
ENST00000648825.1:n.1696-73_1696-72insCTA
ENST00000648916.1:n.2967-73_2967-72insCTA
ENST00000649146.1:n.2126_2127insCTA
ENST00000649607.1:c.3140-73_3140-72insCTA
ENST00000649775.1:c.1453-81_1453-80insCTA
ENST00000650226.1:c.4956-73_4956-72insCTA	ENSP00000496981.1:n.4956-73_4956-72insCTA
ENST00000281928.7:c.4956-73_4956-72insCTA	ENSP00000281928.3:n.4956-73_4956-72insCTA
ENST00000549786.1:c.320-73_320-72insCTA
NM_015335.4:c.4956-73_4956-72insCTA	NP_056150.1:n.4956-73_4956-72insCTA
XM_011538080.1:c.4956-73_4956-72insCTA	XP_011536382.1:n.4956-73_4956-72insCTA
XM_011538081.1:c.4953-73_4953-72insCTA	XP_011536383.1:n.4953-73_4953-72insCTA
XM_011538082.1:c.4926-73_4926-72insCTA	XP_011536384.1:n.4926-73_4926-72insCTA
XM_011538080.2:c.4956-73_4956-72insCTA	XP_011536382.1:n.4956-73_4956-72insCTA
XM_011538081.2:c.4953-73_4953-72insCTA	XP_011536383.1:n.4953-73_4953-72insCTA
XM_011538082.2:c.4926-73_4926-72insCTA	XP_011536384.1:n.4926-73_4926-72insCTA
XM_017019090.1:c.4953-73_4953-72insCTA	XP_016874579.1:n.4953-73_4953-72insCTA
NM_015335.5:c.4956-73_4956-72insCTA MANE Select	NP_056150.1:n.4956-73_4956-72insCTA