Canonical Allele Identifier: CA386881442

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420380G>T (hg19) ; chr12:g.115982575G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982575G>T , CM000674.2:g.115982575G>T	GRCh38
NC_000012.11:g.116420380G>T , CM000674.1:g.116420380G>T	GRCh37
NC_000012.10:g.114904763G>T	NCBI36
NG_023366.1:g.299612C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4984C>A MANE Select	ENSP00000281928.3:p.Pro1662Thr
ENST00000549786.2:c.4412C>A
ENST00000648379.1:n.3352C>A
ENST00000648737.1:n.4748C>A
ENST00000648825.1:n.1724C>A
ENST00000648916.1:n.2995C>A
ENST00000649146.1:n.2227C>A
ENST00000649607.1:c.3168C>A
ENST00000649775.1:c.1473C>A
ENST00000650226.1:c.4984C>A	ENSP00000496981.1:p.Pro1662Thr
ENST00000281928.7:c.4984C>A	ENSP00000281928.3:p.Pro1662Thr
ENST00000549786.1:c.348C>A
ENST00000552340.1:c.16C>A	ENSP00000449876.1:p.Pro6Thr
NM_015335.4:c.4984C>A	NP_056150.1:p.Pro1662Thr
XM_011538080.1:c.4984C>A	XP_011536382.1:p.Pro1662Thr
XM_011538081.1:c.4981C>A	XP_011536383.1:p.Pro1661Thr
XM_011538082.1:c.4954C>A	XP_011536384.1:p.Pro1652Thr
XM_011538080.2:c.4984C>A	XP_011536382.1:p.Pro1662Thr
XM_011538081.2:c.4981C>A	XP_011536383.1:p.Pro1661Thr
XM_011538082.2:c.4954C>A	XP_011536384.1:p.Pro1652Thr
XM_017019090.1:c.4981C>A	XP_016874579.1:p.Pro1661Thr
NM_015335.5:c.4984C>A MANE Select	NP_056150.1:p.Pro1662Thr