Canonical Allele Identifier: CA481944882

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116413112C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975307C>G , CM000674.2:g.115975307C>G	GRCh38
NC_000012.11:g.116413112C>G , CM000674.1:g.116413112C>G	GRCh37
NC_000012.10:g.114897495C>G	NCBI36
NG_023366.1:g.306880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5595G>C MANE Select	ENSP00000281928.3:p.Arg1865=
ENST00000548694.2:n.585G>C
ENST00000648379.1:n.3963G>C
ENST00000648737.1:n.5359G>C
ENST00000648825.1:n.3780G>C
ENST00000648916.1:n.3606G>C
ENST00000649607.1:c.3779G>C
ENST00000649775.1:c.2084G>C
ENST00000650226.1:c.5631G>C	ENSP00000496981.1:p.Arg1877=
ENST00000281928.7:c.5595G>C	ENSP00000281928.3:p.Arg1865=
ENST00000548694.1:n.585G>C
ENST00000552447.1:c.208G>C
NM_015335.4:c.5595G>C	NP_056150.1:p.Arg1865=
XM_011538080.1:c.5631G>C	XP_011536382.1:p.Arg1877=
XM_011538081.1:c.5628G>C	XP_011536383.1:p.Arg1876=
XM_011538082.1:c.5601G>C	XP_011536384.1:p.Arg1867=
XM_011538080.2:c.5631G>C	XP_011536382.1:p.Arg1877=
XM_011538081.2:c.5628G>C	XP_011536383.1:p.Arg1876=
XM_011538082.2:c.5601G>C	XP_011536384.1:p.Arg1867=
XM_017019090.1:c.5592G>C	XP_016874579.1:p.Arg1864=
NM_015335.5:c.5595G>C MANE Select	NP_056150.1:p.Arg1865=