Canonical Allele Identifier: CA6811832
Gene: MED13L HGNC NCBI

Linked Data

dbSNP Id: rs779461762

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116237747T>C , CM000674.2:g.116237747T>C GRCh38
NC_000012.11:g.116675552T>C , CM000674.1:g.116675552T>C GRCh37
NC_000012.10:g.115159935T>C NCBI36
NG_023366.1:g.44440A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.73-42A>G MANE Select ENSP00000281928.3:n.73-42A>G
ENST00000548743.2:c.43-42A>G ENSP00000448553.2:n.43-42A>G
ENST00000551197.2:c.23-42A>G
ENST00000650226.1:c.73-42A>G ENSP00000496981.1:n.73-42A>G
ENST00000650375.1:n.235-42A>G
ENST00000281928.7:c.73-42A>G ENSP00000281928.3:n.73-42A>G
ENST00000548743.1:c.43-42A>G ENSP00000448553.1:n.43-42A>G
ENST00000551197.1:n.23-42A>G
NM_015335.4:c.73-42A>G NP_056150.1:n.73-42A>G
XM_011538080.1:c.73-42A>G XP_011536382.1:n.73-42A>G
XM_011538081.1:c.73-42A>G XP_011536383.1:n.73-42A>G
XM_011538082.1:c.43-42A>G XP_011536384.1:n.43-42A>G
XM_011538080.2:c.73-42A>G XP_011536382.1:n.73-42A>G
XM_011538081.2:c.73-42A>G XP_011536383.1:n.73-42A>G
XM_011538082.2:c.43-42A>G XP_011536384.1:n.43-42A>G
XM_017019090.1:c.73-42A>G XP_016874579.1:n.73-42A>G
NM_015335.5:c.73-42A>G MANE Select NP_056150.1:n.73-42A>G