Canonical Allele Identifier: CA386878872
Gene: MED13L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115975527G>T , CM000674.2:g.115975527G>T GRCh38
NC_000012.11:g.116413332G>T , CM000674.1:g.116413332G>T GRCh37
NC_000012.10:g.114897715G>T NCBI36
NG_023366.1:g.306660C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.5576C>A MANE Select ENSP00000281928.3:p.Ala1859Asp
ENST00000548694.2:n.365C>A
ENST00000648379.1:n.3944C>A
ENST00000648737.1:n.5340C>A
ENST00000648825.1:n.3761C>A
ENST00000648916.1:n.3587C>A
ENST00000649607.1:c.3760C>A
ENST00000649775.1:c.2065C>A
ENST00000650226.1:c.5576C>A ENSP00000496981.1:p.Ala1859Asp
ENST00000281928.7:c.5576C>A ENSP00000281928.3:p.Ala1859Asp
ENST00000548694.1:n.365C>A
ENST00000552447.1:c.153C>A
NM_015335.4:c.5576C>A NP_056150.1:p.Ala1859Asp
XM_011538080.1:c.5576C>A XP_011536382.1:p.Ala1859Asp
XM_011538081.1:c.5573C>A XP_011536383.1:p.Ala1858Asp
XM_011538082.1:c.5546C>A XP_011536384.1:p.Ala1849Asp
XM_011538080.2:c.5576C>A XP_011536382.1:p.Ala1859Asp
XM_011538081.2:c.5573C>A XP_011536383.1:p.Ala1858Asp
XM_011538082.2:c.5546C>A XP_011536384.1:p.Ala1849Asp
XM_017019090.1:c.5573C>A XP_016874579.1:p.Ala1858Asp
NM_015335.5:c.5576C>A MANE Select NP_056150.1:p.Ala1859Asp