Canonical Allele Identifier: CA393129040
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180847T>G , CM000677.2:g.74180847T>G GRCh38
NC_000015.9:g.74473188T>G , CM000677.1:g.74473188T>G GRCh37
NC_000015.8:g.72260241T>G NCBI36
NG_009207.1:g.33184A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1775A>C MANE Select ENSP00000378537.4:p.Gln592Pro
ENST00000323940.9:c.1775A>C ENSP00000326085.5:p.Gln592Pro
ENST00000395105.8:c.1775A>C ENSP00000378537.4:p.Gln592Pro
ENST00000416286.7:c.1751A>C ENSP00000400403.3:p.Gln584Pro
ENST00000423167.6:c.1748A>C ENSP00000413012.2:p.Gln583Pro
ENST00000449139.6:c.1775A>C ENSP00000410221.2:p.Gln592Pro
ENST00000535552.5:c.1886A>C ENSP00000440238.1:p.Gln629Pro
ENST00000545137.5:n.1484A>C
ENST00000563965.5:c.1892A>C ENSP00000456609.1:p.Gln631Pro
ENST00000572785.1:c.630A>C
ENST00000574278.5:c.1820A>C ENSP00000458827.1:p.Gln607Pro
ENST00000574439.5:n.2047A>C
ENST00000616000.4:c.1775A>C ENSP00000479112.1:p.Gln592Pro
NM_001142617.1:c.1775A>C NP_001136089.1:p.Gln592Pro
NM_001142618.1:c.1775A>C NP_001136090.1:p.Gln592Pro
NM_001142619.1:c.1748A>C NP_001136091.1:p.Gln583Pro
NM_001199040.1:c.1886A>C NP_001185969.1:p.Gln629Pro
NM_001199041.1:c.1820A>C NP_001185970.1:p.Gln607Pro
NM_001199042.1:c.1892A>C NP_001185971.1:p.Gln631Pro
NM_022369.3:c.1775A>C NP_071764.3:p.Gln592Pro
XM_011521883.1:c.1775A>C XP_011520185.1:p.Gln592Pro
XM_011521884.1:c.1586A>C XP_011520186.1:p.Gln529Pro
XM_017022478.1:c.1823A>C XP_016877967.1:p.Gln608Pro
XM_017022479.1:c.1775A>C XP_016877968.1:p.Gln592Pro
XM_017022480.1:c.1586A>C XP_016877969.1:p.Gln529Pro
NM_022369.4:c.1775A>C MANE Select NP_071764.3:p.Gln592Pro
NM_001142617.2:c.1775A>C NP_001136089.1:p.Gln592Pro
NM_001142619.2:c.1748A>C NP_001136091.1:p.Gln583Pro
NM_001199042.2:c.1892A>C NP_001185971.1:p.Gln631Pro
NM_001142618.2:c.1775A>C NP_001136090.1:p.Gln592Pro
NM_001199040.2:c.1886A>C NP_001185969.1:p.Gln629Pro
NM_001199041.2:c.1820A>C NP_001185970.1:p.Gln607Pro