Canonical Allele Identifier: CA393128322
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180172G>C , CM000677.2:g.74180172G>C GRCh38
NC_000015.9:g.74472513G>C , CM000677.1:g.74472513G>C GRCh37
NC_000015.8:g.72259566G>C NCBI36
NG_009207.1:g.33859C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1912C>G MANE Select ENSP00000378537.4:p.Arg638Gly
ENST00000323940.9:c.1912C>G ENSP00000326085.5:p.Arg638Gly
ENST00000395105.8:c.1912C>G ENSP00000378537.4:p.Arg638Gly
ENST00000416286.7:c.1888C>G ENSP00000400403.3:p.Arg630Gly
ENST00000423167.6:c.1885C>G ENSP00000413012.2:p.Arg629Gly
ENST00000449139.6:c.1912C>G ENSP00000410221.2:p.Arg638Gly
ENST00000535552.5:c.2023C>G ENSP00000440238.1:p.Arg675Gly
ENST00000545137.5:n.1621C>G
ENST00000563965.5:c.2029C>G ENSP00000456609.1:p.Arg677Gly
ENST00000572785.1:c.767C>G
ENST00000574278.5:c.1957C>G ENSP00000458827.1:p.Arg653Gly
ENST00000574439.5:n.2184C>G
ENST00000616000.4:c.1912C>G ENSP00000479112.1:p.Arg638Gly
NM_001142617.1:c.1912C>G NP_001136089.1:p.Arg638Gly
NM_001142618.1:c.1912C>G NP_001136090.1:p.Arg638Gly
NM_001142619.1:c.1885C>G NP_001136091.1:p.Arg629Gly
NM_001199040.1:c.2023C>G NP_001185969.1:p.Arg675Gly
NM_001199041.1:c.1957C>G NP_001185970.1:p.Arg653Gly
NM_001199042.1:c.2029C>G NP_001185971.1:p.Arg677Gly
NM_022369.3:c.1912C>G NP_071764.3:p.Arg638Gly
XM_011521883.1:c.1912C>G XP_011520185.1:p.Arg638Gly
XM_011521884.1:c.1723C>G XP_011520186.1:p.Arg575Gly
XM_017022478.1:c.1960C>G XP_016877967.1:p.Arg654Gly
XM_017022479.1:c.1912C>G XP_016877968.1:p.Arg638Gly
XM_017022480.1:c.1723C>G XP_016877969.1:p.Arg575Gly
NM_022369.4:c.1912C>G MANE Select NP_071764.3:p.Arg638Gly
NM_001142617.2:c.1912C>G NP_001136089.1:p.Arg638Gly
NM_001142619.2:c.1885C>G NP_001136091.1:p.Arg629Gly
NM_001199042.2:c.2029C>G NP_001185971.1:p.Arg677Gly
NM_001142618.2:c.1912C>G NP_001136090.1:p.Arg638Gly
NM_001199040.2:c.2023C>G NP_001185969.1:p.Arg675Gly
NM_001199041.2:c.1957C>G NP_001185970.1:p.Arg653Gly