Canonical Allele Identifier: CA16606071
Gene: MED13L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.116277089C>A , CM000674.2:g.116277089C>A GRCh38
NC_000012.11:g.116714894C>A , CM000674.1:g.116714894C>A GRCh37
NC_000012.10:g.115199277C>A NCBI36
NG_023366.1:g.5098G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.43G>T MANE Select ENSP00000281928.3:p.Glu15Ter
ENST00000650226.1:c.43G>T ENSP00000496981.1:p.Glu15Ter
ENST00000281928.7:c.43G>T ENSP00000281928.3:p.Glu15Ter
NM_015335.4:c.43G>T NP_056150.1:p.Glu15Ter
XM_011538080.1:c.43G>T XP_011536382.1:p.Glu15Ter
XM_011538081.1:c.43G>T XP_011536383.1:p.Glu15Ter
XM_011538080.2:c.43G>T XP_011536382.1:p.Glu15Ter
XM_011538081.2:c.43G>T XP_011536383.1:p.Glu15Ter
XM_017019090.1:c.43G>T XP_016874579.1:p.Glu15Ter
NM_015335.5:c.43G>T MANE Select NP_056150.1:p.Glu15Ter
Search 100 bp 5'
Search 100 bp 3'