Canonical Allele Identifier: CA393129403
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74181360T>G , CM000677.2:g.74181360T>G GRCh38
NC_000015.9:g.74473701T>G , CM000677.1:g.74473701T>G GRCh37
NC_000015.8:g.72260754T>G NCBI36
NG_009207.1:g.32671A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1619A>C MANE Select ENSP00000378537.4:p.Asn540Thr
ENST00000323940.9:c.1619A>C ENSP00000326085.5:p.Asn540Thr
ENST00000395105.8:c.1619A>C ENSP00000378537.4:p.Asn540Thr
ENST00000416286.7:c.1595A>C ENSP00000400403.3:p.Asn532Thr
ENST00000423167.6:c.1592A>C ENSP00000413012.2:p.Asn531Thr
ENST00000449139.6:c.1619A>C ENSP00000410221.2:p.Asn540Thr
ENST00000535552.5:c.1730A>C ENSP00000440238.1:p.Asn577Thr
ENST00000545137.5:n.1328A>C
ENST00000563965.5:c.1736A>C ENSP00000456609.1:p.Asn579Thr
ENST00000572785.1:c.474A>C
ENST00000574278.5:c.1664A>C ENSP00000458827.1:p.Asn555Thr
ENST00000574439.5:n.1891A>C
ENST00000616000.4:c.1619A>C ENSP00000479112.1:p.Asn540Thr
NM_001142617.1:c.1619A>C NP_001136089.1:p.Asn540Thr
NM_001142618.1:c.1619A>C NP_001136090.1:p.Asn540Thr
NM_001142619.1:c.1592A>C NP_001136091.1:p.Asn531Thr
NM_001199040.1:c.1730A>C NP_001185969.1:p.Asn577Thr
NM_001199041.1:c.1664A>C NP_001185970.1:p.Asn555Thr
NM_001199042.1:c.1736A>C NP_001185971.1:p.Asn579Thr
NM_022369.3:c.1619A>C NP_071764.3:p.Asn540Thr
XM_011521883.1:c.1619A>C XP_011520185.1:p.Asn540Thr
XM_011521884.1:c.1430A>C XP_011520186.1:p.Asn477Thr
XM_017022478.1:c.1667A>C XP_016877967.1:p.Asn556Thr
XM_017022479.1:c.1619A>C XP_016877968.1:p.Asn540Thr
XM_017022480.1:c.1430A>C XP_016877969.1:p.Asn477Thr
NM_022369.4:c.1619A>C MANE Select NP_071764.3:p.Asn540Thr
NM_001142617.2:c.1619A>C NP_001136089.1:p.Asn540Thr
NM_001142619.2:c.1592A>C NP_001136091.1:p.Asn531Thr
NM_001199042.2:c.1736A>C NP_001185971.1:p.Asn579Thr
NM_001142618.2:c.1619A>C NP_001136090.1:p.Asn540Thr
NM_001199040.2:c.1730A>C NP_001185969.1:p.Asn577Thr
NM_001199041.2:c.1664A>C NP_001185970.1:p.Asn555Thr