Canonical Allele Identifier: CA6810768

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115983479G>A , CM000674.2:g.115983479G>A	GRCh38
NC_000012.11:g.116421284G>A , CM000674.1:g.116421284G>A	GRCh37
NC_000012.10:g.114905667G>A	NCBI36
NG_023366.1:g.298708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4593C>T MANE Select	ENSP00000281928.3:p.Thr1531=
ENST00000549786.2:c.4021C>T
ENST00000648379.1:n.2961C>T
ENST00000648737.1:n.4357C>T
ENST00000648825.1:n.1333C>T
ENST00000648916.1:n.2604C>T
ENST00000649146.1:n.1323C>T
ENST00000649607.1:c.2777C>T
ENST00000649775.1:c.1090C>T
ENST00000650226.1:c.4593C>T	ENSP00000496981.1:p.Thr1531=
ENST00000281928.7:c.4593C>T	ENSP00000281928.3:p.Thr1531=
NM_015335.4:c.4593C>T	NP_056150.1:p.Thr1531=
XM_011538080.1:c.4593C>T	XP_011536382.1:p.Thr1531=
XM_011538081.1:c.4590C>T	XP_011536383.1:p.Thr1530=
XM_011538082.1:c.4563C>T	XP_011536384.1:p.Thr1521=
XM_011538080.2:c.4593C>T	XP_011536382.1:p.Thr1531=
XM_011538081.2:c.4590C>T	XP_011536383.1:p.Thr1530=
XM_011538082.2:c.4563C>T	XP_011536384.1:p.Thr1521=
XM_017019090.1:c.4590C>T	XP_016874579.1:p.Thr1530=
NM_015335.5:c.4593C>T MANE Select	NP_056150.1:p.Thr1531=