Canonical Allele Identifier: CA2259193742
Gene: STARD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39651445A>T , CM000679.2:g.39651445A>T GRCh38
NC_000017.10:g.37807698A>T , CM000679.1:g.37807698A>T GRCh37
NC_000017.9:g.35061224A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336308.10:c.-51-2036A>T MANE Select ENSP00000337446.5:n.-51-2036A>T
ENST00000336308.9:c.-51-2036A>T ENSP00000337446.5:n.-51-2036A>T
ENST00000394250.8:c.-51-2036A>T ENSP00000377794.4:n.-51-2036A>T
ENST00000544210.6:c.-51-2036A>T ENSP00000439869.2:n.-51-2036A>T
ENST00000577248.5:c.-16-2071A>T ENSP00000463460.1:n.-16-2071A>T
ENST00000578232.5:n.143-2173A>T
ENST00000578254.5:n.93-2036A>T
ENST00000578577.5:c.-51-2036A>T ENSP00000464472.1:n.-51-2036A>T
ENST00000579479.5:c.-142-310A>T ENSP00000462483.1:n.-142-310A>T
ENST00000580551.5:n.94-2036A>T
ENST00000580611.5:c.-51-2036A>T ENSP00000463613.1:n.-51-2036A>T
ENST00000581894.5:c.-145-307A>T ENSP00000462859.1:n.-145-307A>T
ENST00000583582.5:n.91-2036A>T
ENST00000583718.5:c.-51-2036A>T ENSP00000464204.1:n.-51-2036A>T
ENST00000585214.5:n.71-2036A>T
NM_001165937.1:c.-51-2036A>T NP_001159409.1:n.-51-2036A>T
NM_001165938.1:c.-51-2036A>T NP_001159410.1:n.-51-2036A>T
NM_006804.3:c.-51-2036A>T NP_006795.3:n.-51-2036A>T
XM_006721646.2:c.-51-2036A>T XP_006721709.1:n.-51-2036A>T
XM_011524210.1:c.-51-2036A>T XP_011522512.1:n.-51-2036A>T
XM_011524213.1:c.-51-2036A>T XP_011522515.1:n.-51-2036A>T
XR_934353.1:n.92-2036A>T
XR_934354.1:n.92-2036A>T
XR_934355.1:n.92-2036A>T
NM_006804.4:c.-51-2036A>T MANE Select NP_006795.3:n.-51-2036A>T
NM_001165937.2:c.-51-2036A>T NP_001159409.1:n.-51-2036A>T
NM_001165938.2:c.-51-2036A>T NP_001159410.1:n.-51-2036A>T