Canonical Allele Identifier: CA386881029

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420212T>C (hg19) ; chr12:g.115982407T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982407T>C , CM000674.2:g.115982407T>C	GRCh38
NC_000012.11:g.116420212T>C , CM000674.1:g.116420212T>C	GRCh37
NC_000012.10:g.114904595T>C	NCBI36
NG_023366.1:g.299780A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5152A>G MANE Select	ENSP00000281928.3:p.Met1718Val
ENST00000549786.2:c.4580A>G
ENST00000648379.1:n.3520A>G
ENST00000648737.1:n.4916A>G
ENST00000648825.1:n.1892A>G
ENST00000648916.1:n.3163A>G
ENST00000649146.1:n.2395A>G
ENST00000649607.1:c.3336A>G
ENST00000649775.1:c.1641A>G
ENST00000650226.1:c.5152A>G	ENSP00000496981.1:p.Met1718Val
ENST00000281928.7:c.5152A>G	ENSP00000281928.3:p.Met1718Val
ENST00000549786.1:c.516A>G
ENST00000552340.1:c.184A>G	ENSP00000449876.1:p.Met62Val
NM_015335.4:c.5152A>G	NP_056150.1:p.Met1718Val
XM_011538080.1:c.5152A>G	XP_011536382.1:p.Met1718Val
XM_011538081.1:c.5149A>G	XP_011536383.1:p.Met1717Val
XM_011538082.1:c.5122A>G	XP_011536384.1:p.Met1708Val
XM_011538080.2:c.5152A>G	XP_011536382.1:p.Met1718Val
XM_011538081.2:c.5149A>G	XP_011536383.1:p.Met1717Val
XM_011538082.2:c.5122A>G	XP_011536384.1:p.Met1708Val
XM_017019090.1:c.5149A>G	XP_016874579.1:p.Met1717Val
NM_015335.5:c.5152A>G MANE Select	NP_056150.1:p.Met1718Val