Canonical Allele Identifier: CA386882254

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420388A>C (hg19) ; chr12:g.115982583A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982583A>C , CM000674.2:g.115982583A>C	GRCh38
NC_000012.11:g.116420388A>C , CM000674.1:g.116420388A>C	GRCh37
NC_000012.10:g.114904771A>C	NCBI36
NG_023366.1:g.299604T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4976T>G MANE Select	ENSP00000281928.3:p.Ile1659Arg
ENST00000549786.2:c.4404T>G
ENST00000648379.1:n.3344T>G
ENST00000648737.1:n.4740T>G
ENST00000648825.1:n.1716T>G
ENST00000648916.1:n.2987T>G
ENST00000649146.1:n.2219T>G
ENST00000649607.1:c.3160T>G
ENST00000649775.1:c.1465T>G
ENST00000650226.1:c.4976T>G	ENSP00000496981.1:p.Ile1659Arg
ENST00000281928.7:c.4976T>G	ENSP00000281928.3:p.Ile1659Arg
ENST00000549786.1:c.340T>G
ENST00000552340.1:c.8T>G	ENSP00000449876.1:p.Ile3Arg
NM_015335.4:c.4976T>G	NP_056150.1:p.Ile1659Arg
XM_011538080.1:c.4976T>G	XP_011536382.1:p.Ile1659Arg
XM_011538081.1:c.4973T>G	XP_011536383.1:p.Ile1658Arg
XM_011538082.1:c.4946T>G	XP_011536384.1:p.Ile1649Arg
XM_011538080.2:c.4976T>G	XP_011536382.1:p.Ile1659Arg
XM_011538081.2:c.4973T>G	XP_011536383.1:p.Ile1658Arg
XM_011538082.2:c.4946T>G	XP_011536384.1:p.Ile1649Arg
XM_017019090.1:c.4973T>G	XP_016874579.1:p.Ile1658Arg
NM_015335.5:c.4976T>G MANE Select	NP_056150.1:p.Ile1659Arg