Canonical Allele Identifier: CA2065396922
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997217C= , CM000674.2:g.115997217C= GRCh38
NC_000012.11:g.116435022C= , CM000674.1:g.116435022C= GRCh37
NC_000012.10:g.114919405C= NCBI36
NG_023366.1:g.284970G=

Transcript Alleles

HGVS Amino-acid change
ENST00000281928.9:c.2583G= MANE Select ENSP00000281928.3:p.Leu861=
ENST00000548743.2:c.2553G= ENSP00000448553.2:p.Leu851=
ENST00000549786.2:c.2011G=
ENST00000647927.1:n.2956G=
ENST00000648173.1:n.1378G=
ENST00000648379.1:n.951G=
ENST00000648737.1:n.2347G=
ENST00000648916.1:n.594G=
ENST00000649607.1:c.767G=
ENST00000650226.1:c.2583G= ENSP00000496981.1:p.Leu861=
ENST00000281928.7:c.2583G= ENSP00000281928.3:p.Leu861=
NM_015335.4:c.2583G= NP_056150.1:p.Leu861=
XM_011538080.1:c.2583G= XP_011536382.1:p.Leu861=
XM_011538081.1:c.2580G= XP_011536383.1:p.Leu860=
XM_011538082.1:c.2553G= XP_011536384.1:p.Leu851=
XM_011538080.2:c.2583G= XP_011536382.1:p.Leu861=
XM_011538081.2:c.2580G= XP_011536383.1:p.Leu860=
XM_011538082.2:c.2553G= XP_011536384.1:p.Leu851=
XM_017019090.1:c.2580G= XP_016874579.1:p.Leu860=
NM_015335.5:c.2583G= MANE Select NP_056150.1:p.Leu861=