Canonical Allele Identifier: CA481945967

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420231C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982426C>T , CM000674.2:g.115982426C>T	GRCh38
NC_000012.11:g.116420231C>T , CM000674.1:g.116420231C>T	GRCh37
NC_000012.10:g.114904614C>T	NCBI36
NG_023366.1:g.299761G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5133G>A MANE Select	ENSP00000281928.3:p.Leu1711=
ENST00000549786.2:c.4561G>A
ENST00000648379.1:n.3501G>A
ENST00000648737.1:n.4897G>A
ENST00000648825.1:n.1873G>A
ENST00000648916.1:n.3144G>A
ENST00000649146.1:n.2376G>A
ENST00000649607.1:c.3317G>A
ENST00000649775.1:c.1622G>A
ENST00000650226.1:c.5133G>A	ENSP00000496981.1:p.Leu1711=
ENST00000281928.7:c.5133G>A	ENSP00000281928.3:p.Leu1711=
ENST00000549786.1:c.497G>A
ENST00000552340.1:c.165G>A	ENSP00000449876.1:p.Leu55=
NM_015335.4:c.5133G>A	NP_056150.1:p.Leu1711=
XM_011538080.1:c.5133G>A	XP_011536382.1:p.Leu1711=
XM_011538081.1:c.5130G>A	XP_011536383.1:p.Leu1710=
XM_011538082.1:c.5103G>A	XP_011536384.1:p.Leu1701=
XM_011538080.2:c.5133G>A	XP_011536382.1:p.Leu1711=
XM_011538081.2:c.5130G>A	XP_011536383.1:p.Leu1710=
XM_011538082.2:c.5103G>A	XP_011536384.1:p.Leu1701=
XM_017019090.1:c.5130G>A	XP_016874579.1:p.Leu1710=
NM_015335.5:c.5133G>A MANE Select	NP_056150.1:p.Leu1711=