Canonical Allele Identifier: CA386879111

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975601G>T , CM000674.2:g.115975601G>T	GRCh38
NC_000012.11:g.116413406G>T , CM000674.1:g.116413406G>T	GRCh37
NC_000012.10:g.114897789G>T	NCBI36
NG_023366.1:g.306586C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5502C>A MANE Select	ENSP00000281928.3:p.His1834Gln
ENST00000548694.2:n.291C>A
ENST00000648379.1:n.3870C>A
ENST00000648737.1:n.5266C>A
ENST00000648825.1:n.3687C>A
ENST00000648916.1:n.3513C>A
ENST00000649607.1:c.3686C>A
ENST00000649775.1:c.1991C>A
ENST00000650226.1:c.5502C>A	ENSP00000496981.1:p.His1834Gln
ENST00000281928.7:c.5502C>A	ENSP00000281928.3:p.His1834Gln
ENST00000548694.1:n.291C>A
ENST00000552447.1:c.79C>A
NM_015335.4:c.5502C>A	NP_056150.1:p.His1834Gln
XM_011538080.1:c.5502C>A	XP_011536382.1:p.His1834Gln
XM_011538081.1:c.5499C>A	XP_011536383.1:p.His1833Gln
XM_011538082.1:c.5472C>A	XP_011536384.1:p.His1824Gln
XM_011538080.2:c.5502C>A	XP_011536382.1:p.His1834Gln
XM_011538081.2:c.5499C>A	XP_011536383.1:p.His1833Gln
XM_011538082.2:c.5472C>A	XP_011536384.1:p.His1824Gln
XM_017019090.1:c.5499C>A	XP_016874579.1:p.His1833Gln
NM_015335.5:c.5502C>A MANE Select	NP_056150.1:p.His1834Gln