Canonical Allele Identifier: CA2621143351

Gene: MED13L

Linked Data

• gnomAD v4: 12-115970836-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970836C>T , CM000674.2:g.115970836C>T	GRCh38
NC_000012.11:g.116408641C>T , CM000674.1:g.116408641C>T	GRCh37
NC_000012.10:g.114893024C>T	NCBI36
NG_023366.1:g.311351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5891-66G>A MANE Select	ENSP00000281928.3:n.5891-66G>A
ENST00000548694.2:n.881-66G>A
ENST00000548784.2:n.2105-66G>A
ENST00000648379.1:n.4259-66G>A
ENST00000648737.1:n.5655-66G>A
ENST00000648825.1:n.4076-66G>A
ENST00000648916.1:n.3902-66G>A
ENST00000649607.1:c.4075-66G>A
ENST00000649775.1:c.2380-66G>A
ENST00000650226.1:c.5927-66G>A	ENSP00000496981.1:n.5927-66G>A
ENST00000281928.7:c.5891-66G>A	ENSP00000281928.3:n.5891-66G>A
ENST00000548784.1:n.389-66G>A
ENST00000552447.1:c.504-66G>A
NM_015335.4:c.5891-66G>A	NP_056150.1:n.5891-66G>A
XM_011538080.1:c.5927-66G>A	XP_011536382.1:n.5927-66G>A
XM_011538081.1:c.5924-66G>A	XP_011536383.1:n.5924-66G>A
XM_011538082.1:c.5897-66G>A	XP_011536384.1:n.5897-66G>A
XM_011538080.2:c.5927-66G>A	XP_011536382.1:n.5927-66G>A
XM_011538081.2:c.5924-66G>A	XP_011536383.1:n.5924-66G>A
XM_011538082.2:c.5897-66G>A	XP_011536384.1:n.5897-66G>A
XM_017019090.1:c.5888-66G>A	XP_016874579.1:n.5888-66G>A
NM_015335.5:c.5891-66G>A MANE Select	NP_056150.1:n.5891-66G>A