Canonical Allele Identifier: CA2621142336

Gene: MED13L

Linked Data

• gnomAD v4: 12-115984516-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984516_115984517insG , CM000674.2:g.115984516_115984517insG	GRCh38
NC_000012.11:g.116422321_116422322insG , CM000674.1:g.116422321_116422322insG	GRCh37
NC_000012.10:g.114906704_114906705insG	NCBI36
NG_023366.1:g.297670_297671insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-145_4339-144insC MANE Select	ENSP00000281928.3:n.4339-145_4339-144insC
ENST00000549786.2:c.3767-145_3767-144insC
ENST00000648379.1:n.2707-145_2707-144insC
ENST00000648737.1:n.4103-145_4103-144insC
ENST00000648825.1:n.1079-145_1079-144insC
ENST00000648916.1:n.2350-145_2350-144insC
ENST00000649146.1:n.924_925insC
ENST00000649607.1:c.2523-145_2523-144insC
ENST00000649775.1:c.836-145_836-144insC
ENST00000650091.1:n.2315-145_2315-144insC
ENST00000650226.1:c.4339-145_4339-144insC	ENSP00000496981.1:n.4339-145_4339-144insC
ENST00000281928.7:c.4339-145_4339-144insC	ENSP00000281928.3:n.4339-145_4339-144insC
NM_015335.4:c.4339-145_4339-144insC	NP_056150.1:n.4339-145_4339-144insC
XM_011538080.1:c.4339-145_4339-144insC	XP_011536382.1:n.4339-145_4339-144insC
XM_011538081.1:c.4336-145_4336-144insC	XP_011536383.1:n.4336-145_4336-144insC
XM_011538082.1:c.4309-145_4309-144insC	XP_011536384.1:n.4309-145_4309-144insC
XM_011538080.2:c.4339-145_4339-144insC	XP_011536382.1:n.4339-145_4339-144insC
XM_011538081.2:c.4336-145_4336-144insC	XP_011536383.1:n.4336-145_4336-144insC
XM_011538082.2:c.4309-145_4309-144insC	XP_011536384.1:n.4309-145_4309-144insC
XM_017019090.1:c.4336-145_4336-144insC	XP_016874579.1:n.4336-145_4336-144insC
NM_015335.5:c.4339-145_4339-144insC MANE Select	NP_056150.1:n.4339-145_4339-144insC