Canonical Allele Identifier: CA386888420
Gene: MED13L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115991680G>C , CM000674.2:g.115991680G>C GRCh38
NC_000012.11:g.116429485G>C , CM000674.1:g.116429485G>C GRCh37
NC_000012.10:g.114913868G>C NCBI36
NG_023366.1:g.290507C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.3274C>G MANE Select ENSP00000281928.3:p.Leu1092Val
ENST00000548743.2:c.3244C>G
ENST00000549786.2:c.2702C>G
ENST00000648379.1:n.1642C>G
ENST00000648737.1:n.3038C>G
ENST00000648825.1:n.14C>G
ENST00000648916.1:n.1285C>G
ENST00000649607.1:c.1458C>G
ENST00000650226.1:c.3274C>G ENSP00000496981.1:p.Leu1092Val
ENST00000281928.7:c.3274C>G ENSP00000281928.3:p.Leu1092Val
NM_015335.4:c.3274C>G NP_056150.1:p.Leu1092Val
XM_011538080.1:c.3274C>G XP_011536382.1:p.Leu1092Val
XM_011538081.1:c.3271C>G XP_011536383.1:p.Leu1091Val
XM_011538082.1:c.3244C>G XP_011536384.1:p.Leu1082Val
XM_011538080.2:c.3274C>G XP_011536382.1:p.Leu1092Val
XM_011538081.2:c.3271C>G XP_011536383.1:p.Leu1091Val
XM_011538082.2:c.3244C>G XP_011536384.1:p.Leu1082Val
XM_017019090.1:c.3271C>G XP_016874579.1:p.Leu1091Val
NM_015335.5:c.3274C>G MANE Select NP_056150.1:p.Leu1092Val