Canonical Allele Identifier: CA386881251

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420308T>C (hg19) ; chr12:g.115982503T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982503T>C , CM000674.2:g.115982503T>C	GRCh38
NC_000012.11:g.116420308T>C , CM000674.1:g.116420308T>C	GRCh37
NC_000012.10:g.114904691T>C	NCBI36
NG_023366.1:g.299684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5056A>G MANE Select	ENSP00000281928.3:p.Thr1686Ala
ENST00000549786.2:c.4484A>G
ENST00000648379.1:n.3424A>G
ENST00000648737.1:n.4820A>G
ENST00000648825.1:n.1796A>G
ENST00000648916.1:n.3067A>G
ENST00000649146.1:n.2299A>G
ENST00000649607.1:c.3240A>G
ENST00000649775.1:c.1545A>G
ENST00000650226.1:c.5056A>G	ENSP00000496981.1:p.Thr1686Ala
ENST00000281928.7:c.5056A>G	ENSP00000281928.3:p.Thr1686Ala
ENST00000549786.1:c.420A>G
ENST00000552340.1:c.88A>G	ENSP00000449876.1:p.Thr30Ala
NM_015335.4:c.5056A>G	NP_056150.1:p.Thr1686Ala
XM_011538080.1:c.5056A>G	XP_011536382.1:p.Thr1686Ala
XM_011538081.1:c.5053A>G	XP_011536383.1:p.Thr1685Ala
XM_011538082.1:c.5026A>G	XP_011536384.1:p.Thr1676Ala
XM_011538080.2:c.5056A>G	XP_011536382.1:p.Thr1686Ala
XM_011538081.2:c.5053A>G	XP_011536383.1:p.Thr1685Ala
XM_011538082.2:c.5026A>G	XP_011536384.1:p.Thr1676Ala
XM_017019090.1:c.5053A>G	XP_016874579.1:p.Thr1685Ala
NM_015335.5:c.5056A>G MANE Select	NP_056150.1:p.Thr1686Ala