Canonical Allele Identifier: CA481943191

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408477A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970672A>G , CM000674.2:g.115970672A>G	GRCh38
NC_000012.11:g.116408477A>G , CM000674.1:g.116408477A>G	GRCh37
NC_000012.10:g.114892860A>G	NCBI36
NG_023366.1:g.311515T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5989T>C MANE Select	ENSP00000281928.3:p.Leu1997=
ENST00000548784.2:n.2203T>C
ENST00000648379.1:n.4357T>C
ENST00000648737.1:n.5753T>C
ENST00000648825.1:n.4174T>C
ENST00000648916.1:n.4000T>C
ENST00000649607.1:c.4173T>C
ENST00000649775.1:c.2478T>C
ENST00000650226.1:c.6025T>C	ENSP00000496981.1:p.Leu2009=
ENST00000281928.7:c.5989T>C	ENSP00000281928.3:p.Leu1997=
NM_015335.4:c.5989T>C	NP_056150.1:p.Leu1997=
XM_011538080.1:c.6025T>C	XP_011536382.1:p.Leu2009=
XM_011538081.1:c.6022T>C	XP_011536383.1:p.Leu2008=
XM_011538082.1:c.5995T>C	XP_011536384.1:p.Leu1999=
XM_011538080.2:c.6025T>C	XP_011536382.1:p.Leu2009=
XM_011538081.2:c.6022T>C	XP_011536383.1:p.Leu2008=
XM_011538082.2:c.5995T>C	XP_011536384.1:p.Leu1999=
XM_017019090.1:c.5986T>C	XP_016874579.1:p.Leu1996=
NM_015335.5:c.5989T>C MANE Select	NP_056150.1:p.Leu1997=