Canonical Allele Identifier: CA386881219

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420294C>G (hg19) ; chr12:g.115982489C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982489C>G , CM000674.2:g.115982489C>G	GRCh38
NC_000012.11:g.116420294C>G , CM000674.1:g.116420294C>G	GRCh37
NC_000012.10:g.114904677C>G	NCBI36
NG_023366.1:g.299698G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5070G>C MANE Select	ENSP00000281928.3:p.Glu1690Asp
ENST00000549786.2:c.4498G>C
ENST00000648379.1:n.3438G>C
ENST00000648737.1:n.4834G>C
ENST00000648825.1:n.1810G>C
ENST00000648916.1:n.3081G>C
ENST00000649146.1:n.2313G>C
ENST00000649607.1:c.3254G>C
ENST00000649775.1:c.1559G>C
ENST00000650226.1:c.5070G>C	ENSP00000496981.1:p.Glu1690Asp
ENST00000281928.7:c.5070G>C	ENSP00000281928.3:p.Glu1690Asp
ENST00000549786.1:c.434G>C
ENST00000552340.1:c.102G>C	ENSP00000449876.1:p.Glu34Asp
NM_015335.4:c.5070G>C	NP_056150.1:p.Glu1690Asp
XM_011538080.1:c.5070G>C	XP_011536382.1:p.Glu1690Asp
XM_011538081.1:c.5067G>C	XP_011536383.1:p.Glu1689Asp
XM_011538082.1:c.5040G>C	XP_011536384.1:p.Glu1680Asp
XM_011538080.2:c.5070G>C	XP_011536382.1:p.Glu1690Asp
XM_011538081.2:c.5067G>C	XP_011536383.1:p.Glu1689Asp
XM_011538082.2:c.5040G>C	XP_011536384.1:p.Glu1680Asp
XM_017019090.1:c.5067G>C	XP_016874579.1:p.Glu1689Asp
NM_015335.5:c.5070G>C MANE Select	NP_056150.1:p.Glu1690Asp