Canonical Allele Identifier: CA386890639

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434908C>G (hg19) ; chr12:g.115997103C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997103C>G , CM000674.2:g.115997103C>G	GRCh38
NC_000012.11:g.116434908C>G , CM000674.1:g.116434908C>G	GRCh37
NC_000012.10:g.114919291C>G	NCBI36
NG_023366.1:g.285084G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2697G>C MANE Select	ENSP00000281928.3:p.Glu899Asp
ENST00000548743.2:c.2667G>C	ENSP00000448553.2:p.Glu889Asp
ENST00000549786.2:c.2125G>C
ENST00000647927.1:n.3070G>C
ENST00000648173.1:n.1492G>C
ENST00000648379.1:n.1065G>C
ENST00000648737.1:n.2461G>C
ENST00000648916.1:n.708G>C
ENST00000649607.1:c.881G>C
ENST00000650226.1:c.2697G>C	ENSP00000496981.1:p.Glu899Asp
ENST00000281928.7:c.2697G>C	ENSP00000281928.3:p.Glu899Asp
NM_015335.4:c.2697G>C	NP_056150.1:p.Glu899Asp
XM_011538080.1:c.2697G>C	XP_011536382.1:p.Glu899Asp
XM_011538081.1:c.2694G>C	XP_011536383.1:p.Glu898Asp
XM_011538082.1:c.2667G>C	XP_011536384.1:p.Glu889Asp
XM_011538080.2:c.2697G>C	XP_011536382.1:p.Glu899Asp
XM_011538081.2:c.2694G>C	XP_011536383.1:p.Glu898Asp
XM_011538082.2:c.2667G>C	XP_011536384.1:p.Glu889Asp
XM_017019090.1:c.2694G>C	XP_016874579.1:p.Glu898Asp
NM_015335.5:c.2697G>C MANE Select	NP_056150.1:p.Glu899Asp