Canonical Allele Identifier: CA386887736

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429319A>G (hg19) ; chr12:g.115991514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991514A>G , CM000674.2:g.115991514A>G	GRCh38
NC_000012.11:g.116429319A>G , CM000674.1:g.116429319A>G	GRCh37
NC_000012.10:g.114913702A>G	NCBI36
NG_023366.1:g.290673T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3440T>C MANE Select	ENSP00000281928.3:p.Leu1147Pro
ENST00000549786.2:c.2868T>C
ENST00000648379.1:n.1808T>C
ENST00000648737.1:n.3204T>C
ENST00000648825.1:n.180T>C
ENST00000648916.1:n.1451T>C
ENST00000649607.1:c.1624T>C
ENST00000650226.1:c.3440T>C	ENSP00000496981.1:p.Leu1147Pro
ENST00000281928.7:c.3440T>C	ENSP00000281928.3:p.Leu1147Pro
NM_015335.4:c.3440T>C	NP_056150.1:p.Leu1147Pro
XM_011538080.1:c.3440T>C	XP_011536382.1:p.Leu1147Pro
XM_011538081.1:c.3437T>C	XP_011536383.1:p.Leu1146Pro
XM_011538082.1:c.3410T>C	XP_011536384.1:p.Leu1137Pro
XM_011538080.2:c.3440T>C	XP_011536382.1:p.Leu1147Pro
XM_011538081.2:c.3437T>C	XP_011536383.1:p.Leu1146Pro
XM_011538082.2:c.3410T>C	XP_011536384.1:p.Leu1137Pro
XM_017019090.1:c.3437T>C	XP_016874579.1:p.Leu1146Pro
NM_015335.5:c.3440T>C MANE Select	NP_056150.1:p.Leu1147Pro