Canonical Allele Identifier: CA386927715

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116675504G>C (hg19) ; chr12:g.116237699G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237699G>C , CM000674.2:g.116237699G>C	GRCh38
NC_000012.11:g.116675504G>C , CM000674.1:g.116675504G>C	GRCh37
NC_000012.10:g.115159887G>C	NCBI36
NG_023366.1:g.44488C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.79C>G MANE Select	ENSP00000281928.3:p.Leu27Val
ENST00000548743.2:c.49C>G	ENSP00000448553.2:p.Leu17Val
ENST00000551197.2:c.29C>G
ENST00000650226.1:c.79C>G	ENSP00000496981.1:p.Leu27Val
ENST00000650375.1:n.241C>G
ENST00000281928.7:c.79C>G	ENSP00000281928.3:p.Leu27Val
ENST00000548743.1:c.49C>G	ENSP00000448553.1:p.Leu17Val
ENST00000551197.1:n.29C>G
NM_015335.4:c.79C>G	NP_056150.1:p.Leu27Val
XM_011538080.1:c.79C>G	XP_011536382.1:p.Leu27Val
XM_011538081.1:c.79C>G	XP_011536383.1:p.Leu27Val
XM_011538082.1:c.49C>G	XP_011536384.1:p.Leu17Val
XM_011538080.2:c.79C>G	XP_011536382.1:p.Leu27Val
XM_011538081.2:c.79C>G	XP_011536383.1:p.Leu27Val
XM_011538082.2:c.49C>G	XP_011536384.1:p.Leu17Val
XM_017019090.1:c.79C>G	XP_016874579.1:p.Leu27Val
NM_015335.5:c.79C>G MANE Select	NP_056150.1:p.Leu27Val