Canonical Allele Identifier: CA386883695

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116422101G>T (hg19) ; chr12:g.115984296G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984296G>T , CM000674.2:g.115984296G>T	GRCh38
NC_000012.11:g.116422101G>T , CM000674.1:g.116422101G>T	GRCh37
NC_000012.10:g.114906484G>T	NCBI36
NG_023366.1:g.297891C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4415C>A MANE Select	ENSP00000281928.3:p.Ala1472Glu
ENST00000549786.2:c.3843C>A
ENST00000648379.1:n.2783C>A
ENST00000648737.1:n.4179C>A
ENST00000648825.1:n.1155C>A
ENST00000648916.1:n.2426C>A
ENST00000649146.1:n.1145C>A
ENST00000649607.1:c.2599C>A
ENST00000649775.1:c.912C>A
ENST00000650091.1:n.2391C>A
ENST00000650226.1:c.4415C>A	ENSP00000496981.1:p.Ala1472Glu
ENST00000281928.7:c.4415C>A	ENSP00000281928.3:p.Ala1472Glu
NM_015335.4:c.4415C>A	NP_056150.1:p.Ala1472Glu
XM_011538080.1:c.4415C>A	XP_011536382.1:p.Ala1472Glu
XM_011538081.1:c.4412C>A	XP_011536383.1:p.Ala1471Glu
XM_011538082.1:c.4385C>A	XP_011536384.1:p.Ala1462Glu
XM_011538080.2:c.4415C>A	XP_011536382.1:p.Ala1472Glu
XM_011538081.2:c.4412C>A	XP_011536383.1:p.Ala1471Glu
XM_011538082.2:c.4385C>A	XP_011536384.1:p.Ala1462Glu
XM_017019090.1:c.4412C>A	XP_016874579.1:p.Ala1471Glu
NM_015335.5:c.4415C>A MANE Select	NP_056150.1:p.Ala1472Glu