Canonical Allele Identifier: CA386890800
Gene: MED13L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997171A>C , CM000674.2:g.115997171A>C GRCh38
NC_000012.11:g.116434976A>C , CM000674.1:g.116434976A>C GRCh37
NC_000012.10:g.114919359A>C NCBI36
NG_023366.1:g.285016T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.2629T>G MANE Select ENSP00000281928.3:p.Phe877Val
ENST00000548743.2:c.2599T>G ENSP00000448553.2:p.Phe867Val
ENST00000549786.2:c.2057T>G
ENST00000647927.1:n.3002T>G
ENST00000648173.1:n.1424T>G
ENST00000648379.1:n.997T>G
ENST00000648737.1:n.2393T>G
ENST00000648916.1:n.640T>G
ENST00000649607.1:c.813T>G
ENST00000650226.1:c.2629T>G ENSP00000496981.1:p.Phe877Val
ENST00000281928.7:c.2629T>G ENSP00000281928.3:p.Phe877Val
NM_015335.4:c.2629T>G NP_056150.1:p.Phe877Val
XM_011538080.1:c.2629T>G XP_011536382.1:p.Phe877Val
XM_011538081.1:c.2626T>G XP_011536383.1:p.Phe876Val
XM_011538082.1:c.2599T>G XP_011536384.1:p.Phe867Val
XM_011538080.2:c.2629T>G XP_011536382.1:p.Phe877Val
XM_011538081.2:c.2626T>G XP_011536383.1:p.Phe876Val
XM_011538082.2:c.2599T>G XP_011536384.1:p.Phe867Val
XM_017019090.1:c.2626T>G XP_016874579.1:p.Phe876Val
NM_015335.5:c.2629T>G MANE Select NP_056150.1:p.Phe877Val