Canonical Allele Identifier: CA2621142259

Gene: MED13L

Linked Data

• gnomAD v4: 12-115984387-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984387_115984388insC , CM000674.2:g.115984387_115984388insC	GRCh38
NC_000012.11:g.116422192_116422193insC , CM000674.1:g.116422192_116422193insC	GRCh37
NC_000012.10:g.114906575_114906576insC	NCBI36
NG_023366.1:g.297799_297800insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-16_4339-15insG MANE Select	ENSP00000281928.3:n.4339-16_4339-15insG
ENST00000549786.2:c.3767-16_3767-15insG
ENST00000648379.1:n.2707-16_2707-15insG
ENST00000648737.1:n.4103-16_4103-15insG
ENST00000648825.1:n.1079-16_1079-15insG
ENST00000648916.1:n.2350-16_2350-15insG
ENST00000649146.1:n.1053_1054insG
ENST00000649607.1:c.2523-16_2523-15insG
ENST00000649775.1:c.836-16_836-15insG
ENST00000650091.1:n.2315-16_2315-15insG
ENST00000650226.1:c.4339-16_4339-15insG	ENSP00000496981.1:n.4339-16_4339-15insG
ENST00000281928.7:c.4339-16_4339-15insG	ENSP00000281928.3:n.4339-16_4339-15insG
NM_015335.4:c.4339-16_4339-15insG	NP_056150.1:n.4339-16_4339-15insG
XM_011538080.1:c.4339-16_4339-15insG	XP_011536382.1:n.4339-16_4339-15insG
XM_011538081.1:c.4336-16_4336-15insG	XP_011536383.1:n.4336-16_4336-15insG
XM_011538082.1:c.4309-16_4309-15insG	XP_011536384.1:n.4309-16_4309-15insG
XM_011538080.2:c.4339-16_4339-15insG	XP_011536382.1:n.4339-16_4339-15insG
XM_011538081.2:c.4336-16_4336-15insG	XP_011536383.1:n.4336-16_4336-15insG
XM_011538082.2:c.4309-16_4309-15insG	XP_011536384.1:n.4309-16_4309-15insG
XM_017019090.1:c.4336-16_4336-15insG	XP_016874579.1:n.4336-16_4336-15insG
NM_015335.5:c.4339-16_4339-15insG MANE Select	NP_056150.1:n.4339-16_4339-15insG