Canonical Allele Identifier: CA482137134

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429383T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991578T>G , CM000674.2:g.115991578T>G	GRCh38
NC_000012.11:g.116429383T>G , CM000674.1:g.116429383T>G	GRCh37
NC_000012.10:g.114913766T>G	NCBI36
NG_023366.1:g.290609A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3376A>C MANE Select	ENSP00000281928.3:p.Arg1126=
ENST00000549786.2:c.2804A>C
ENST00000648379.1:n.1744A>C
ENST00000648737.1:n.3140A>C
ENST00000648825.1:n.116A>C
ENST00000648916.1:n.1387A>C
ENST00000649607.1:c.1560A>C
ENST00000650226.1:c.3376A>C	ENSP00000496981.1:p.Arg1126=
ENST00000281928.7:c.3376A>C	ENSP00000281928.3:p.Arg1126=
NM_015335.4:c.3376A>C	NP_056150.1:p.Arg1126=
XM_011538080.1:c.3376A>C	XP_011536382.1:p.Arg1126=
XM_011538081.1:c.3373A>C	XP_011536383.1:p.Arg1125=
XM_011538082.1:c.3346A>C	XP_011536384.1:p.Arg1116=
XM_011538080.2:c.3376A>C	XP_011536382.1:p.Arg1126=
XM_011538081.2:c.3373A>C	XP_011536383.1:p.Arg1125=
XM_011538082.2:c.3346A>C	XP_011536384.1:p.Arg1116=
XM_017019090.1:c.3373A>C	XP_016874579.1:p.Arg1125=
NM_015335.5:c.3376A>C MANE Select	NP_056150.1:p.Arg1126=