Canonical Allele Identifier: CA386888187

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429437T>G (hg19) ; chr12:g.115991632T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991632T>G , CM000674.2:g.115991632T>G	GRCh38
NC_000012.11:g.116429437T>G , CM000674.1:g.116429437T>G	GRCh37
NC_000012.10:g.114913820T>G	NCBI36
NG_023366.1:g.290555A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3322A>C MANE Select	ENSP00000281928.3:p.Ser1108Arg
ENST00000549786.2:c.2750A>C
ENST00000648379.1:n.1690A>C
ENST00000648737.1:n.3086A>C
ENST00000648825.1:n.62A>C
ENST00000648916.1:n.1333A>C
ENST00000649607.1:c.1506A>C
ENST00000650226.1:c.3322A>C	ENSP00000496981.1:p.Ser1108Arg
ENST00000281928.7:c.3322A>C	ENSP00000281928.3:p.Ser1108Arg
NM_015335.4:c.3322A>C	NP_056150.1:p.Ser1108Arg
XM_011538080.1:c.3322A>C	XP_011536382.1:p.Ser1108Arg
XM_011538081.1:c.3319A>C	XP_011536383.1:p.Ser1107Arg
XM_011538082.1:c.3292A>C	XP_011536384.1:p.Ser1098Arg
XM_011538080.2:c.3322A>C	XP_011536382.1:p.Ser1108Arg
XM_011538081.2:c.3319A>C	XP_011536383.1:p.Ser1107Arg
XM_011538082.2:c.3292A>C	XP_011536384.1:p.Ser1098Arg
XM_017019090.1:c.3319A>C	XP_016874579.1:p.Ser1107Arg
NM_015335.5:c.3322A>C MANE Select	NP_056150.1:p.Ser1108Arg