Canonical Allele Identifier: CA2083177972
Gene: STARD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33129928T= , CM000675.2:g.33129928T= GRCh38
NC_000013.10:g.33704065T= , CM000675.1:g.33704065T= GRCh37
NC_000013.9:g.32602065T= NCBI36
NG_029752.1:g.160837A=
NG_029752.2:g.551908A=

Transcript Alleles

HGVS Amino-acid Change
NM_178006.4:c.749A= MANE Select NP_821074.1:p.Lys250=
ENST00000336934.10:c.749A= MANE Select ENSP00000338785.4:p.Lys250=
NM_001243466.1:c.725A= NP_001230395.1:p.Lys242=
NM_001243466.2:c.725A= NP_001230395.1:p.Lys242=
NM_001243474.1:c.395A= NP_001230403.1:p.Lys132=
NM_001243474.2:c.395A= NP_001230403.1:p.Lys132=
NM_001243476.2:c.644A= NP_001230405.1:p.Lys215=
NM_001243476.3:c.644A= NP_001230405.1:p.Lys215=
NM_052851.2:c.395A= NP_443083.1:p.Lys132=
NM_052851.3:c.395A= NP_443083.1:p.Lys132=
NM_178006.3:c.749A= NP_821074.1:p.Lys250=
NM_178007.2:c.725A= NP_821075.1:p.Lys242=
NM_178007.3:c.725A= NP_821075.1:p.Lys242=
ENST00000255486.8:c.725A= ENSP00000255486.4:p.Lys242=
ENST00000336934.9:c.749A= ENSP00000338785.4:p.Lys250=
ENST00000399365.7:c.395A= ENSP00000382300.3:p.Lys132=
ENST00000567873.1:c.704A= ENSP00000456233.1:p.Lys235=
ENST00000567873.2:c.704A= ENSP00000456233.2:p.Lys235=
XM_011535298.1:c.782A= XP_011533600.1:p.Lys261=
XM_011535299.1:c.644A= XP_011533601.1:p.Lys215=
XM_011535299.3:c.644A= XP_011533601.1:p.Lys215=
XM_017020834.2:c.704A= XP_016876323.1:p.Lys235=
XM_017020835.2:c.644A= XP_016876324.1:p.Lys215=
XM_024449429.1:c.644A= XP_024305197.1:p.Lys215=