Canonical Allele Identifier: CA481944611

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116412992G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975187G>A , CM000674.2:g.115975187G>A	GRCh38
NC_000012.11:g.116412992G>A , CM000674.1:g.116412992G>A	GRCh37
NC_000012.10:g.114897375G>A	NCBI36
NG_023366.1:g.307000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5715C>T MANE Select	ENSP00000281928.3:p.Gly1905=
ENST00000548694.2:n.705C>T
ENST00000648379.1:n.4083C>T
ENST00000648737.1:n.5479C>T
ENST00000648825.1:n.3900C>T
ENST00000648916.1:n.3726C>T
ENST00000649607.1:c.3899C>T
ENST00000649775.1:c.2204C>T
ENST00000650226.1:c.5751C>T	ENSP00000496981.1:p.Gly1917=
ENST00000281928.7:c.5715C>T	ENSP00000281928.3:p.Gly1905=
ENST00000548694.1:n.705C>T
ENST00000552447.1:c.328C>T
NM_015335.4:c.5715C>T	NP_056150.1:p.Gly1905=
XM_011538080.1:c.5751C>T	XP_011536382.1:p.Gly1917=
XM_011538081.1:c.5748C>T	XP_011536383.1:p.Gly1916=
XM_011538082.1:c.5721C>T	XP_011536384.1:p.Gly1907=
XM_011538080.2:c.5751C>T	XP_011536382.1:p.Gly1917=
XM_011538081.2:c.5748C>T	XP_011536383.1:p.Gly1916=
XM_011538082.2:c.5721C>T	XP_011536384.1:p.Gly1907=
XM_017019090.1:c.5712C>T	XP_016874579.1:p.Gly1904=
NM_015335.5:c.5715C>T MANE Select	NP_056150.1:p.Gly1905=