Canonical Allele Identifier: CA386927554

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116675431G>A (hg19) ; chr12:g.116237626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237626G>A , CM000674.2:g.116237626G>A	GRCh38
NC_000012.11:g.116675431G>A , CM000674.1:g.116675431G>A	GRCh37
NC_000012.10:g.115159814G>A	NCBI36
NG_023366.1:g.44561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.152C>T MANE Select	ENSP00000281928.3:p.Ala51Val
ENST00000548743.2:c.122C>T	ENSP00000448553.2:p.Ala41Val
ENST00000551197.2:c.102C>T
ENST00000647567.1:c.62C>T	ENSP00000497136.1:p.Ala21Val
ENST00000650226.1:c.152C>T	ENSP00000496981.1:p.Ala51Val
ENST00000650375.1:n.314C>T
ENST00000281928.7:c.152C>T	ENSP00000281928.3:p.Ala51Val
ENST00000548743.1:c.122C>T	ENSP00000448553.1:p.Ala41Val
ENST00000551197.1:n.102C>T
NM_015335.4:c.152C>T	NP_056150.1:p.Ala51Val
XM_011538080.1:c.152C>T	XP_011536382.1:p.Ala51Val
XM_011538081.1:c.152C>T	XP_011536383.1:p.Ala51Val
XM_011538082.1:c.122C>T	XP_011536384.1:p.Ala41Val
XM_011538080.2:c.152C>T	XP_011536382.1:p.Ala51Val
XM_011538081.2:c.152C>T	XP_011536383.1:p.Ala51Val
XM_011538082.2:c.122C>T	XP_011536384.1:p.Ala41Val
XM_017019090.1:c.152C>T	XP_016874579.1:p.Ala51Val
NM_015335.5:c.152C>T MANE Select	NP_056150.1:p.Ala51Val