Canonical Allele Identifier: CA386883653

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116422083T>G (hg19) ; chr12:g.115984278T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984278T>G , CM000674.2:g.115984278T>G	GRCh38
NC_000012.11:g.116422083T>G , CM000674.1:g.116422083T>G	GRCh37
NC_000012.10:g.114906466T>G	NCBI36
NG_023366.1:g.297909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4433A>C MANE Select	ENSP00000281928.3:p.Glu1478Ala
ENST00000549786.2:c.3861A>C
ENST00000648379.1:n.2801A>C
ENST00000648737.1:n.4197A>C
ENST00000648825.1:n.1173A>C
ENST00000648916.1:n.2444A>C
ENST00000649146.1:n.1163A>C
ENST00000649607.1:c.2617A>C
ENST00000649775.1:c.930A>C
ENST00000650091.1:n.2409A>C
ENST00000650226.1:c.4433A>C	ENSP00000496981.1:p.Glu1478Ala
ENST00000281928.7:c.4433A>C	ENSP00000281928.3:p.Glu1478Ala
NM_015335.4:c.4433A>C	NP_056150.1:p.Glu1478Ala
XM_011538080.1:c.4433A>C	XP_011536382.1:p.Glu1478Ala
XM_011538081.1:c.4430A>C	XP_011536383.1:p.Glu1477Ala
XM_011538082.1:c.4403A>C	XP_011536384.1:p.Glu1468Ala
XM_011538080.2:c.4433A>C	XP_011536382.1:p.Glu1478Ala
XM_011538081.2:c.4430A>C	XP_011536383.1:p.Glu1477Ala
XM_011538082.2:c.4403A>C	XP_011536384.1:p.Glu1468Ala
XM_017019090.1:c.4430A>C	XP_016874579.1:p.Glu1477Ala
NM_015335.5:c.4433A>C MANE Select	NP_056150.1:p.Glu1478Ala