Canonical Allele Identifier: CA386878114

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116412984T>G (hg19) ; chr12:g.115975179T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975179T>G , CM000674.2:g.115975179T>G	GRCh38
NC_000012.11:g.116412984T>G , CM000674.1:g.116412984T>G	GRCh37
NC_000012.10:g.114897367T>G	NCBI36
NG_023366.1:g.307008A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5723A>C MANE Select	ENSP00000281928.3:p.Glu1908Ala
ENST00000548694.2:n.713A>C
ENST00000648379.1:n.4091A>C
ENST00000648737.1:n.5487A>C
ENST00000648825.1:n.3908A>C
ENST00000648916.1:n.3734A>C
ENST00000649607.1:c.3907A>C
ENST00000649775.1:c.2212A>C
ENST00000650226.1:c.5759A>C	ENSP00000496981.1:p.Glu1920Ala
ENST00000281928.7:c.5723A>C	ENSP00000281928.3:p.Glu1908Ala
ENST00000548694.1:n.713A>C
ENST00000552447.1:c.336A>C
NM_015335.4:c.5723A>C	NP_056150.1:p.Glu1908Ala
XM_011538080.1:c.5759A>C	XP_011536382.1:p.Glu1920Ala
XM_011538081.1:c.5756A>C	XP_011536383.1:p.Glu1919Ala
XM_011538082.1:c.5729A>C	XP_011536384.1:p.Glu1910Ala
XM_011538080.2:c.5759A>C	XP_011536382.1:p.Glu1920Ala
XM_011538081.2:c.5756A>C	XP_011536383.1:p.Glu1919Ala
XM_011538082.2:c.5729A>C	XP_011536384.1:p.Glu1910Ala
XM_017019090.1:c.5720A>C	XP_016874579.1:p.Glu1907Ala
NM_015335.5:c.5723A>C MANE Select	NP_056150.1:p.Glu1908Ala