Canonical Allele Identifier: CA386876416

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408512A>G (hg19) ; chr12:g.115970707A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970707A>G , CM000674.2:g.115970707A>G	GRCh38
NC_000012.11:g.116408512A>G , CM000674.1:g.116408512A>G	GRCh37
NC_000012.10:g.114892895A>G	NCBI36
NG_023366.1:g.311480T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.5954T>C MANE Select	ENSP00000281928.3:p.Leu1985Pro
ENST00000548784.2:n.2168T>C
ENST00000648379.1:n.4322T>C
ENST00000648737.1:n.5718T>C
ENST00000648825.1:n.4139T>C
ENST00000648916.1:n.3965T>C
ENST00000649607.1:c.4138T>C
ENST00000649775.1:c.2443T>C
ENST00000650226.1:c.5990T>C	ENSP00000496981.1:p.Leu1997Pro
ENST00000281928.7:c.5954T>C	ENSP00000281928.3:p.Leu1985Pro
ENST00000548784.1:n.452T>C
ENST00000552447.1:c.567T>C
NM_015335.4:c.5954T>C	NP_056150.1:p.Leu1985Pro
XM_011538080.1:c.5990T>C	XP_011536382.1:p.Leu1997Pro
XM_011538081.1:c.5987T>C	XP_011536383.1:p.Leu1996Pro
XM_011538082.1:c.5960T>C	XP_011536384.1:p.Leu1987Pro
XM_011538080.2:c.5990T>C	XP_011536382.1:p.Leu1997Pro
XM_011538081.2:c.5987T>C	XP_011536383.1:p.Leu1996Pro
XM_011538082.2:c.5960T>C	XP_011536384.1:p.Leu1987Pro
XM_017019090.1:c.5951T>C	XP_016874579.1:p.Leu1984Pro
NM_015335.5:c.5954T>C MANE Select	NP_056150.1:p.Leu1985Pro