Canonical Allele Identifier: CA10636551
Gene: STRA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 317091
dbSNP Id: rs182529524

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180005G>T , CM000677.2:g.74180005G>T GRCh38
NC_000015.9:g.74472346G>T , CM000677.1:g.74472346G>T GRCh37
NC_000015.8:g.72259399G>T NCBI36
NG_009207.1:g.34026C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395105.9:c.*75C>A MANE Select ENSP00000378537.4:n.*75C>A
ENST00000323940.9:c.*75C>A ENSP00000326085.5:n.*75C>A
ENST00000395105.8:c.*75C>A ENSP00000378537.4:n.*75C>A
ENST00000416286.7:c.*75C>A ENSP00000400403.3:n.*75C>A
ENST00000423167.6:c.*75C>A ENSP00000413012.2:n.*75C>A
ENST00000449139.6:c.*75C>A ENSP00000410221.2:n.*75C>A
ENST00000535552.5:c.*75C>A ENSP00000440238.1:n.*75C>A
ENST00000545137.5:n.1788C>A
ENST00000563965.5:c.*75C>A ENSP00000456609.1:n.*75C>A
ENST00000574278.5:c.*75C>A ENSP00000458827.1:n.*75C>A
ENST00000574439.5:n.2351C>A
ENST00000616000.4:c.*75C>A ENSP00000479112.1:n.*75C>A
NM_001142617.1:c.*75C>A NP_001136089.1:n.*75C>A
NM_001142618.1:c.*75C>A NP_001136090.1:n.*75C>A
NM_001142619.1:c.*75C>A NP_001136091.1:n.*75C>A
NM_001199040.1:c.*75C>A NP_001185969.1:n.*75C>A
NM_001199041.1:c.*75C>A NP_001185970.1:n.*75C>A
NM_001199042.1:c.*75C>A NP_001185971.1:n.*75C>A
NM_022369.3:c.*75C>A NP_071764.3:n.*75C>A
XM_011521883.1:c.*75C>A XP_011520185.1:n.*75C>A
XM_011521884.1:c.*75C>A XP_011520186.1:n.*75C>A
XM_017022478.1:c.*75C>A XP_016877967.1:n.*75C>A
XM_017022479.1:c.*75C>A XP_016877968.1:n.*75C>A
XM_017022480.1:c.*75C>A XP_016877969.1:n.*75C>A
NM_022369.4:c.*75C>A MANE Select NP_071764.3:n.*75C>A
NM_001142617.2:c.*75C>A NP_001136089.1:n.*75C>A
NM_001142619.2:c.*75C>A NP_001136091.1:n.*75C>A
NM_001199042.2:c.*75C>A NP_001185971.1:n.*75C>A
NM_001142618.2:c.*75C>A NP_001136090.1:n.*75C>A
NM_001199040.2:c.*75C>A NP_001185969.1:n.*75C>A
NM_001199041.2:c.*75C>A NP_001185970.1:n.*75C>A