Canonical Allele Identifier: CA386889933
Gene: MED13L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115996671T>G , CM000674.2:g.115996671T>G GRCh38
NC_000012.11:g.116434476T>G , CM000674.1:g.116434476T>G GRCh37
NC_000012.10:g.114918859T>G NCBI36
NG_023366.1:g.285516A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.2801A>C MANE Select ENSP00000281928.3:p.Tyr934Ser
ENST00000548743.2:c.2771A>C ENSP00000448553.2:p.Tyr924Ser
ENST00000549786.2:c.2229A>C
ENST00000647927.1:n.3174A>C
ENST00000648173.1:n.1596A>C
ENST00000648379.1:n.1169A>C
ENST00000648737.1:n.2565A>C
ENST00000648916.1:n.812A>C
ENST00000649607.1:c.985A>C
ENST00000650226.1:c.2801A>C ENSP00000496981.1:p.Tyr934Ser
ENST00000281928.7:c.2801A>C ENSP00000281928.3:p.Tyr934Ser
NM_015335.4:c.2801A>C NP_056150.1:p.Tyr934Ser
XM_011538080.1:c.2801A>C XP_011536382.1:p.Tyr934Ser
XM_011538081.1:c.2798A>C XP_011536383.1:p.Tyr933Ser
XM_011538082.1:c.2771A>C XP_011536384.1:p.Tyr924Ser
XM_011538080.2:c.2801A>C XP_011536382.1:p.Tyr934Ser
XM_011538081.2:c.2798A>C XP_011536383.1:p.Tyr933Ser
XM_011538082.2:c.2771A>C XP_011536384.1:p.Tyr924Ser
XM_017019090.1:c.2798A>C XP_016874579.1:p.Tyr933Ser
NM_015335.5:c.2801A>C MANE Select NP_056150.1:p.Tyr934Ser