Canonical Allele Identifier: CA2621142256

Gene: MED13L

Linked Data

• gnomAD v4: 12-115984384-G-GTTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984384_115984385insTTAT , CM000674.2:g.115984384_115984385insTTAT	GRCh38
NC_000012.11:g.116422189_116422190insTTAT , CM000674.1:g.116422189_116422190insTTAT	GRCh37
NC_000012.10:g.114906572_114906573insTTAT	NCBI36
NG_023366.1:g.297802_297803insATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-13_4339-12insATAA MANE Select	ENSP00000281928.3:n.4339-13_4339-12insATAA
ENST00000549786.2:c.3767-13_3767-12insATAA
ENST00000648379.1:n.2707-13_2707-12insATAA
ENST00000648737.1:n.4103-13_4103-12insATAA
ENST00000648825.1:n.1079-13_1079-12insATAA
ENST00000648916.1:n.2350-13_2350-12insATAA
ENST00000649146.1:n.1056_1057insATAA
ENST00000649607.1:c.2523-13_2523-12insATAA
ENST00000649775.1:c.836-13_836-12insATAA
ENST00000650091.1:n.2315-13_2315-12insATAA
ENST00000650226.1:c.4339-13_4339-12insATAA	ENSP00000496981.1:n.4339-13_4339-12insATAA
ENST00000281928.7:c.4339-13_4339-12insATAA	ENSP00000281928.3:n.4339-13_4339-12insATAA
NM_015335.4:c.4339-13_4339-12insATAA	NP_056150.1:n.4339-13_4339-12insATAA
XM_011538080.1:c.4339-13_4339-12insATAA	XP_011536382.1:n.4339-13_4339-12insATAA
XM_011538081.1:c.4336-13_4336-12insATAA	XP_011536383.1:n.4336-13_4336-12insATAA
XM_011538082.1:c.4309-13_4309-12insATAA	XP_011536384.1:n.4309-13_4309-12insATAA
XM_011538080.2:c.4339-13_4339-12insATAA	XP_011536382.1:n.4339-13_4339-12insATAA
XM_011538081.2:c.4336-13_4336-12insATAA	XP_011536383.1:n.4336-13_4336-12insATAA
XM_011538082.2:c.4309-13_4309-12insATAA	XP_011536384.1:n.4309-13_4309-12insATAA
XM_017019090.1:c.4336-13_4336-12insATAA	XP_016874579.1:n.4336-13_4336-12insATAA
NM_015335.5:c.4339-13_4339-12insATAA MANE Select	NP_056150.1:n.4339-13_4339-12insATAA