Canonical Allele Identifier: CA481946628

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420348G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982543G>T , CM000674.2:g.115982543G>T	GRCh38
NC_000012.11:g.116420348G>T , CM000674.1:g.116420348G>T	GRCh37
NC_000012.10:g.114904731G>T	NCBI36
NG_023366.1:g.299644C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5016C>A MANE Select	ENSP00000281928.3:p.Ala1672=
ENST00000549786.2:c.4444C>A
ENST00000648379.1:n.3384C>A
ENST00000648737.1:n.4780C>A
ENST00000648825.1:n.1756C>A
ENST00000648916.1:n.3027C>A
ENST00000649146.1:n.2259C>A
ENST00000649607.1:c.3200C>A
ENST00000649775.1:c.1505C>A
ENST00000650226.1:c.5016C>A	ENSP00000496981.1:p.Ala1672=
ENST00000281928.7:c.5016C>A	ENSP00000281928.3:p.Ala1672=
ENST00000549786.1:c.380C>A
ENST00000552340.1:c.48C>A	ENSP00000449876.1:p.Ala16=
NM_015335.4:c.5016C>A	NP_056150.1:p.Ala1672=
XM_011538080.1:c.5016C>A	XP_011536382.1:p.Ala1672=
XM_011538081.1:c.5013C>A	XP_011536383.1:p.Ala1671=
XM_011538082.1:c.4986C>A	XP_011536384.1:p.Ala1662=
XM_011538080.2:c.5016C>A	XP_011536382.1:p.Ala1672=
XM_011538081.2:c.5013C>A	XP_011536383.1:p.Ala1671=
XM_011538082.2:c.4986C>A	XP_011536384.1:p.Ala1662=
XM_017019090.1:c.5013C>A	XP_016874579.1:p.Ala1671=
NM_015335.5:c.5016C>A MANE Select	NP_056150.1:p.Ala1672=