Canonical Allele Identifier: CA1700934293
Gene: STARD3NL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.38201307A>C , CM000669.2:g.38201307A>C GRCh38
NC_000007.13:g.38240908A>C , CM000669.1:g.38240908A>C GRCh37
NC_000007.12:g.38207433A>C NCBI36
NG_030015.1:g.28101A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000009041.12:c.-58-6140A>C MANE Select ENSP00000009041.7:n.-58-6140A>C
ENST00000009041.11:c.-58-6140A>C ENSP00000009041.7:n.-58-6140A>C
ENST00000396013.5:c.-58-6140A>C ENSP00000379334.1:n.-58-6140A>C
ENST00000429075.1:c.-59+2942A>C ENSP00000402028.1:n.-59+2942A>C
ENST00000434197.5:c.-58-6140A>C ENSP00000394000.1:n.-58-6140A>C
ENST00000440144.5:c.-186-763A>C ENSP00000411933.1:n.-186-763A>C
ENST00000453225.5:c.-311-407A>C ENSP00000395455.1:n.-311-407A>C
ENST00000471550.1:n.98-6140A>C
NM_032016.3:c.-58-6140A>C NP_114405.1:n.-58-6140A>C
XM_005249880.1:c.-58-6140A>C XP_005249937.1:n.-58-6140A>C
XM_005249881.1:c.-58-6140A>C XP_005249938.1:n.-58-6140A>C
XM_006715789.1:c.-58-6140A>C XP_006715852.1:n.-58-6140A>C
XM_011515572.1:c.-59+2942A>C XP_011513874.1:n.-59+2942A>C
NM_001363339.1:c.-311-407A>C NP_001350268.1:n.-311-407A>C
NM_001363340.1:c.-58-6140A>C NP_001350269.1:n.-58-6140A>C
NM_001363343.1:c.-311-407A>C NP_001350272.1:n.-311-407A>C
NM_001363344.1:c.-58-6140A>C NP_001350273.1:n.-58-6140A>C
NM_001363345.1:c.-58-6140A>C NP_001350274.1:n.-58-6140A>C
NM_001363346.1:c.-439-407A>C NP_001350275.1:n.-439-407A>C
NM_001363347.1:c.-175-407A>C NP_001350276.1:n.-175-407A>C
XM_017012693.1:c.-175-407A>C XP_016868182.1:n.-175-407A>C
NM_001363339.2:c.-311-407A>C NP_001350268.1:n.-311-407A>C
NM_001363340.2:c.-58-6140A>C NP_001350269.1:n.-58-6140A>C
NM_001363343.2:c.-311-407A>C NP_001350272.1:n.-311-407A>C
NM_001363344.2:c.-58-6140A>C NP_001350273.1:n.-58-6140A>C
NM_001363345.2:c.-58-6140A>C NP_001350274.1:n.-58-6140A>C
NM_001363346.2:c.-439-407A>C NP_001350275.1:n.-439-407A>C
NM_001363347.2:c.-175-407A>C NP_001350276.1:n.-175-407A>C
NM_032016.4:c.-58-6140A>C MANE Select NP_114405.1:n.-58-6140A>C