Canonical Allele Identifier: CA386881199

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420286G>T (hg19) ; chr12:g.115982481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982481G>T , CM000674.2:g.115982481G>T	GRCh38
NC_000012.11:g.116420286G>T , CM000674.1:g.116420286G>T	GRCh37
NC_000012.10:g.114904669G>T	NCBI36
NG_023366.1:g.299706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5078C>A MANE Select	ENSP00000281928.3:p.Ser1693Tyr
ENST00000549786.2:c.4506C>A
ENST00000648379.1:n.3446C>A
ENST00000648737.1:n.4842C>A
ENST00000648825.1:n.1818C>A
ENST00000648916.1:n.3089C>A
ENST00000649146.1:n.2321C>A
ENST00000649607.1:c.3262C>A
ENST00000649775.1:c.1567C>A
ENST00000650226.1:c.5078C>A	ENSP00000496981.1:p.Ser1693Tyr
ENST00000281928.7:c.5078C>A	ENSP00000281928.3:p.Ser1693Tyr
ENST00000549786.1:c.442C>A
ENST00000552340.1:c.110C>A	ENSP00000449876.1:p.Ser37Tyr
NM_015335.4:c.5078C>A	NP_056150.1:p.Ser1693Tyr
XM_011538080.1:c.5078C>A	XP_011536382.1:p.Ser1693Tyr
XM_011538081.1:c.5075C>A	XP_011536383.1:p.Ser1692Tyr
XM_011538082.1:c.5048C>A	XP_011536384.1:p.Ser1683Tyr
XM_011538080.2:c.5078C>A	XP_011536382.1:p.Ser1693Tyr
XM_011538081.2:c.5075C>A	XP_011536383.1:p.Ser1692Tyr
XM_011538082.2:c.5048C>A	XP_011536384.1:p.Ser1683Tyr
XM_017019090.1:c.5075C>A	XP_016874579.1:p.Ser1692Tyr
NM_015335.5:c.5078C>A MANE Select	NP_056150.1:p.Ser1693Tyr