Canonical Allele Identifier: CA386882233

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420383T>C (hg19) ; chr12:g.115982578T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982578T>C , CM000674.2:g.115982578T>C	GRCh38
NC_000012.11:g.116420383T>C , CM000674.1:g.116420383T>C	GRCh37
NC_000012.10:g.114904766T>C	NCBI36
NG_023366.1:g.299609A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4981A>G MANE Select	ENSP00000281928.3:p.Ile1661Val
ENST00000549786.2:c.4409A>G
ENST00000648379.1:n.3349A>G
ENST00000648737.1:n.4745A>G
ENST00000648825.1:n.1721A>G
ENST00000648916.1:n.2992A>G
ENST00000649146.1:n.2224A>G
ENST00000649607.1:c.3165A>G
ENST00000649775.1:c.1470A>G
ENST00000650226.1:c.4981A>G	ENSP00000496981.1:p.Ile1661Val
ENST00000281928.7:c.4981A>G	ENSP00000281928.3:p.Ile1661Val
ENST00000549786.1:c.345A>G
ENST00000552340.1:c.13A>G	ENSP00000449876.1:p.Ile5Val
NM_015335.4:c.4981A>G	NP_056150.1:p.Ile1661Val
XM_011538080.1:c.4981A>G	XP_011536382.1:p.Ile1661Val
XM_011538081.1:c.4978A>G	XP_011536383.1:p.Ile1660Val
XM_011538082.1:c.4951A>G	XP_011536384.1:p.Ile1651Val
XM_011538080.2:c.4981A>G	XP_011536382.1:p.Ile1661Val
XM_011538081.2:c.4978A>G	XP_011536383.1:p.Ile1660Val
XM_011538082.2:c.4951A>G	XP_011536384.1:p.Ile1651Val
XM_017019090.1:c.4978A>G	XP_016874579.1:p.Ile1660Val
NM_015335.5:c.4981A>G MANE Select	NP_056150.1:p.Ile1661Val