Canonical Allele Identifier: CA244133373

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115971054C>T , CM000674.2:g.115971054C>T	GRCh38
NC_000012.11:g.116408859C>T , CM000674.1:g.116408859C>T	GRCh37
NC_000012.10:g.114893242C>T	NCBI36
NG_023366.1:g.311133G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015335.5:c.5891-284G>A MANE Select	NP_056150.1:n.5891-284G>A
ENST00000281928.9:c.5891-284G>A MANE Select	ENSP00000281928.3:n.5891-284G>A
NM_015335.4:c.5891-284G>A	NP_056150.1:n.5891-284G>A
ENST00000281928.7:c.5891-284G>A	ENSP00000281928.3:n.5891-284G>A
ENST00000548694.2:n.881-284G>A
ENST00000548784.1:n.389-284G>A
ENST00000548784.2:n.2105-284G>A
ENST00000552447.1:c.504-284G>A
ENST00000648379.1:n.4259-284G>A
ENST00000648737.1:n.5655-284G>A
ENST00000648825.1:n.4076-284G>A
ENST00000648916.1:n.3902-284G>A
ENST00000649607.1:c.4075-284G>A
ENST00000649775.1:c.2380-284G>A
ENST00000650226.1:c.5927-284G>A	ENSP00000496981.1:n.5927-284G>A
XM_011538080.1:c.5927-284G>A	XP_011536382.1:n.5927-284G>A
XM_011538080.2:c.5927-284G>A	XP_011536382.1:n.5927-284G>A
XM_011538081.1:c.5924-284G>A	XP_011536383.1:n.5924-284G>A
XM_011538081.2:c.5924-284G>A	XP_011536383.1:n.5924-284G>A
XM_011538082.1:c.5897-284G>A	XP_011536384.1:n.5897-284G>A
XM_011538082.2:c.5897-284G>A	XP_011536384.1:n.5897-284G>A
XM_017019090.1:c.5888-284G>A	XP_016874579.1:n.5888-284G>A