Canonical Allele Identifier: CA952183617

Gene: MED13L

Linked Data

• dbSNP Id: rs1876529664
• gnomAD v3: 12-115970806-A-T
• gnomAD v4: 12-115970806-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970806A>T , CM000674.2:g.115970806A>T	GRCh38
NC_000012.11:g.116408611A>T , CM000674.1:g.116408611A>T	GRCh37
NC_000012.10:g.114892994A>T	NCBI36
NG_023366.1:g.311381T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5891-36T>A MANE Select	ENSP00000281928.3:n.5891-36T>A
ENST00000548694.2:n.881-36T>A
ENST00000548784.2:n.2105-36T>A
ENST00000648379.1:n.4259-36T>A
ENST00000648737.1:n.5655-36T>A
ENST00000648825.1:n.4076-36T>A
ENST00000648916.1:n.3902-36T>A
ENST00000649607.1:c.4075-36T>A
ENST00000649775.1:c.2380-36T>A
ENST00000650226.1:c.5927-36T>A	ENSP00000496981.1:n.5927-36T>A
ENST00000281928.7:c.5891-36T>A	ENSP00000281928.3:n.5891-36T>A
ENST00000548784.1:n.389-36T>A
ENST00000552447.1:c.504-36T>A
NM_015335.4:c.5891-36T>A	NP_056150.1:n.5891-36T>A
XM_011538080.1:c.5927-36T>A	XP_011536382.1:n.5927-36T>A
XM_011538081.1:c.5924-36T>A	XP_011536383.1:n.5924-36T>A
XM_011538082.1:c.5897-36T>A	XP_011536384.1:n.5897-36T>A
XM_011538080.2:c.5927-36T>A	XP_011536382.1:n.5927-36T>A
XM_011538081.2:c.5924-36T>A	XP_011536383.1:n.5924-36T>A
XM_011538082.2:c.5897-36T>A	XP_011536384.1:n.5897-36T>A
XM_017019090.1:c.5888-36T>A	XP_016874579.1:n.5888-36T>A
NM_015335.5:c.5891-36T>A MANE Select	NP_056150.1:n.5891-36T>A