Canonical Allele Identifier: CA386881410

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420373T>A (hg19) ; chr12:g.115982568T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982568T>A , CM000674.2:g.115982568T>A	GRCh38
NC_000012.11:g.116420373T>A , CM000674.1:g.116420373T>A	GRCh37
NC_000012.10:g.114904756T>A	NCBI36
NG_023366.1:g.299619A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4991A>T MANE Select	ENSP00000281928.3:p.Glu1664Val
ENST00000549786.2:c.4419A>T
ENST00000648379.1:n.3359A>T
ENST00000648737.1:n.4755A>T
ENST00000648825.1:n.1731A>T
ENST00000648916.1:n.3002A>T
ENST00000649146.1:n.2234A>T
ENST00000649607.1:c.3175A>T
ENST00000649775.1:c.1480A>T
ENST00000650226.1:c.4991A>T	ENSP00000496981.1:p.Glu1664Val
ENST00000281928.7:c.4991A>T	ENSP00000281928.3:p.Glu1664Val
ENST00000549786.1:c.355A>T
ENST00000552340.1:c.23A>T	ENSP00000449876.1:p.Glu8Val
NM_015335.4:c.4991A>T	NP_056150.1:p.Glu1664Val
XM_011538080.1:c.4991A>T	XP_011536382.1:p.Glu1664Val
XM_011538081.1:c.4988A>T	XP_011536383.1:p.Glu1663Val
XM_011538082.1:c.4961A>T	XP_011536384.1:p.Glu1654Val
XM_011538080.2:c.4991A>T	XP_011536382.1:p.Glu1664Val
XM_011538081.2:c.4988A>T	XP_011536383.1:p.Glu1663Val
XM_011538082.2:c.4961A>T	XP_011536384.1:p.Glu1654Val
XM_017019090.1:c.4988A>T	XP_016874579.1:p.Glu1663Val
NM_015335.5:c.4991A>T MANE Select	NP_056150.1:p.Glu1664Val