Canonical Allele Identifier: CA386890489

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434871C>G (hg19) ; chr12:g.115997066C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997066C>G , CM000674.2:g.115997066C>G	GRCh38
NC_000012.11:g.116434871C>G , CM000674.1:g.116434871C>G	GRCh37
NC_000012.10:g.114919254C>G	NCBI36
NG_023366.1:g.285121G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2734G>C MANE Select	ENSP00000281928.3:p.Glu912Gln
ENST00000548743.2:c.2704G>C	ENSP00000448553.2:p.Glu902Gln
ENST00000549786.2:c.2162G>C
ENST00000647927.1:n.3107G>C
ENST00000648173.1:n.1529G>C
ENST00000648379.1:n.1102G>C
ENST00000648737.1:n.2498G>C
ENST00000648916.1:n.745G>C
ENST00000649607.1:c.918G>C
ENST00000650226.1:c.2734G>C	ENSP00000496981.1:p.Glu912Gln
ENST00000281928.7:c.2734G>C	ENSP00000281928.3:p.Glu912Gln
NM_015335.4:c.2734G>C	NP_056150.1:p.Glu912Gln
XM_011538080.1:c.2734G>C	XP_011536382.1:p.Glu912Gln
XM_011538081.1:c.2731G>C	XP_011536383.1:p.Glu911Gln
XM_011538082.1:c.2704G>C	XP_011536384.1:p.Glu902Gln
XM_011538080.2:c.2734G>C	XP_011536382.1:p.Glu912Gln
XM_011538081.2:c.2731G>C	XP_011536383.1:p.Glu911Gln
XM_011538082.2:c.2704G>C	XP_011536384.1:p.Glu902Gln
XM_017019090.1:c.2731G>C	XP_016874579.1:p.Glu911Gln
NM_015335.5:c.2734G>C MANE Select	NP_056150.1:p.Glu912Gln