Canonical Allele Identifier: CA15909440

Gene: STARD3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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