Canonical Allele Identifier: CA386882257

Gene: MED13L

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4976T>A MANE Select	ENSP00000281928.3:p.Ile1659Lys
ENST00000549786.2:c.4404T>A
ENST00000648379.1:n.3344T>A
ENST00000648737.1:n.4740T>A
ENST00000648825.1:n.1716T>A
ENST00000648916.1:n.2987T>A
ENST00000649146.1:n.2219T>A
ENST00000649607.1:c.3160T>A
ENST00000649775.1:c.1465T>A
ENST00000650226.1:c.4976T>A	ENSP00000496981.1:p.Ile1659Lys
ENST00000281928.7:c.4976T>A	ENSP00000281928.3:p.Ile1659Lys
ENST00000549786.1:c.340T>A
ENST00000552340.1:c.8T>A	ENSP00000449876.1:p.Ile3Lys
NM_015335.4:c.4976T>A	NP_056150.1:p.Ile1659Lys
XM_011538080.1:c.4976T>A	XP_011536382.1:p.Ile1659Lys
XM_011538081.1:c.4973T>A	XP_011536383.1:p.Ile1658Lys
XM_011538082.1:c.4946T>A	XP_011536384.1:p.Ile1649Lys
XM_011538080.2:c.4976T>A	XP_011536382.1:p.Ile1659Lys
XM_011538081.2:c.4973T>A	XP_011536383.1:p.Ile1658Lys
XM_011538082.2:c.4946T>A	XP_011536384.1:p.Ile1649Lys
XM_017019090.1:c.4973T>A	XP_016874579.1:p.Ile1658Lys
NM_015335.5:c.4976T>A MANE Select	NP_056150.1:p.Ile1659Lys