Canonical Allele Identifier: CA386887506

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429218C>T (hg19) ; chr12:g.115991413C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991413C>T , CM000674.2:g.115991413C>T	GRCh38
NC_000012.11:g.116429218C>T , CM000674.1:g.116429218C>T	GRCh37
NC_000012.10:g.114913601C>T	NCBI36
NG_023366.1:g.290774G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3541G>A MANE Select	ENSP00000281928.3:p.Glu1181Lys
ENST00000549786.2:c.2969G>A
ENST00000648379.1:n.1909G>A
ENST00000648737.1:n.3305G>A
ENST00000648825.1:n.281G>A
ENST00000648916.1:n.1552G>A
ENST00000649607.1:c.1725G>A
ENST00000649775.1:c.38G>A
ENST00000650226.1:c.3541G>A	ENSP00000496981.1:p.Glu1181Lys
ENST00000281928.7:c.3541G>A	ENSP00000281928.3:p.Glu1181Lys
NM_015335.4:c.3541G>A	NP_056150.1:p.Glu1181Lys
XM_011538080.1:c.3541G>A	XP_011536382.1:p.Glu1181Lys
XM_011538081.1:c.3538G>A	XP_011536383.1:p.Glu1180Lys
XM_011538082.1:c.3511G>A	XP_011536384.1:p.Glu1171Lys
XM_011538080.2:c.3541G>A	XP_011536382.1:p.Glu1181Lys
XM_011538081.2:c.3538G>A	XP_011536383.1:p.Glu1180Lys
XM_011538082.2:c.3511G>A	XP_011536384.1:p.Glu1171Lys
XM_017019090.1:c.3538G>A	XP_016874579.1:p.Glu1180Lys
NM_015335.5:c.3541G>A MANE Select	NP_056150.1:p.Glu1181Lys