Canonical Allele Identifier: CA2621143800

Gene: MED13L

Linked Data

• gnomAD v4: 12-115975401-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975401A>G , CM000674.2:g.115975401A>G	GRCh38
NC_000012.11:g.116413206A>G , CM000674.1:g.116413206A>G	GRCh37
NC_000012.10:g.114897589A>G	NCBI36
NG_023366.1:g.306786T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-88T>C MANE Select	ENSP00000281928.3:n.5589-88T>C
ENST00000548694.2:n.491T>C
ENST00000648379.1:n.3957-88T>C
ENST00000648737.1:n.5353-88T>C
ENST00000648825.1:n.3774-88T>C
ENST00000648916.1:n.3600-88T>C
ENST00000649607.1:c.3773-88T>C
ENST00000649775.1:c.2078-88T>C
ENST00000650226.1:c.5589-52T>C	ENSP00000496981.1:n.5589-52T>C
ENST00000281928.7:c.5589-88T>C	ENSP00000281928.3:n.5589-88T>C
ENST00000548694.1:n.491T>C
ENST00000552447.1:c.166-52T>C
NM_015335.4:c.5589-88T>C	NP_056150.1:n.5589-88T>C
XM_011538080.1:c.5589-52T>C	XP_011536382.1:n.5589-52T>C
XM_011538081.1:c.5586-52T>C	XP_011536383.1:n.5586-52T>C
XM_011538082.1:c.5559-52T>C	XP_011536384.1:n.5559-52T>C
XM_011538080.2:c.5589-52T>C	XP_011536382.1:n.5589-52T>C
XM_011538081.2:c.5586-52T>C	XP_011536383.1:n.5586-52T>C
XM_011538082.2:c.5559-52T>C	XP_011536384.1:n.5559-52T>C
XM_017019090.1:c.5586-88T>C	XP_016874579.1:n.5586-88T>C
NM_015335.5:c.5589-88T>C MANE Select	NP_056150.1:n.5589-88T>C