Canonical Allele Identifier: CA386881386

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420367T>G (hg19) ; chr12:g.115982562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982562T>G , CM000674.2:g.115982562T>G	GRCh38
NC_000012.11:g.116420367T>G , CM000674.1:g.116420367T>G	GRCh37
NC_000012.10:g.114904750T>G	NCBI36
NG_023366.1:g.299625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4997A>C MANE Select	ENSP00000281928.3:p.Asp1666Ala
ENST00000549786.2:c.4425A>C
ENST00000648379.1:n.3365A>C
ENST00000648737.1:n.4761A>C
ENST00000648825.1:n.1737A>C
ENST00000648916.1:n.3008A>C
ENST00000649146.1:n.2240A>C
ENST00000649607.1:c.3181A>C
ENST00000649775.1:c.1486A>C
ENST00000650226.1:c.4997A>C	ENSP00000496981.1:p.Asp1666Ala
ENST00000281928.7:c.4997A>C	ENSP00000281928.3:p.Asp1666Ala
ENST00000549786.1:c.361A>C
ENST00000552340.1:c.29A>C	ENSP00000449876.1:p.Asp10Ala
NM_015335.4:c.4997A>C	NP_056150.1:p.Asp1666Ala
XM_011538080.1:c.4997A>C	XP_011536382.1:p.Asp1666Ala
XM_011538081.1:c.4994A>C	XP_011536383.1:p.Asp1665Ala
XM_011538082.1:c.4967A>C	XP_011536384.1:p.Asp1656Ala
XM_011538080.2:c.4997A>C	XP_011536382.1:p.Asp1666Ala
XM_011538081.2:c.4994A>C	XP_011536383.1:p.Asp1665Ala
XM_011538082.2:c.4967A>C	XP_011536384.1:p.Asp1656Ala
XM_017019090.1:c.4994A>C	XP_016874579.1:p.Asp1665Ala
NM_015335.5:c.4997A>C MANE Select	NP_056150.1:p.Asp1666Ala