Canonical Allele Identifier: CA952199592
Gene: MED13L HGNC NCBI

Linked Data

dbSNP Id: rs1870229513

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116237751A>G , CM000674.2:g.116237751A>G GRCh38
NC_000012.11:g.116675556A>G , CM000674.1:g.116675556A>G GRCh37
NC_000012.10:g.115159939A>G NCBI36
NG_023366.1:g.44436T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.73-46T>C MANE Select ENSP00000281928.3:n.73-46T>C
ENST00000548743.2:c.43-46T>C ENSP00000448553.2:n.43-46T>C
ENST00000551197.2:c.23-46T>C
ENST00000650226.1:c.73-46T>C ENSP00000496981.1:n.73-46T>C
ENST00000650375.1:n.235-46T>C
ENST00000281928.7:c.73-46T>C ENSP00000281928.3:n.73-46T>C
ENST00000548743.1:c.43-46T>C ENSP00000448553.1:n.43-46T>C
ENST00000551197.1:n.23-46T>C
NM_015335.4:c.73-46T>C NP_056150.1:n.73-46T>C
XM_011538080.1:c.73-46T>C XP_011536382.1:n.73-46T>C
XM_011538081.1:c.73-46T>C XP_011536383.1:n.73-46T>C
XM_011538082.1:c.43-46T>C XP_011536384.1:n.43-46T>C
XM_011538080.2:c.73-46T>C XP_011536382.1:n.73-46T>C
XM_011538081.2:c.73-46T>C XP_011536383.1:n.73-46T>C
XM_011538082.2:c.43-46T>C XP_011536384.1:n.43-46T>C
XM_017019090.1:c.73-46T>C XP_016874579.1:n.73-46T>C
NM_015335.5:c.73-46T>C MANE Select NP_056150.1:n.73-46T>C