Canonical Allele Identifier: CA393135330
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74190863G>C , CM000677.2:g.74190863G>C GRCh38
NC_000015.9:g.74483204G>C , CM000677.1:g.74483204G>C GRCh37
NC_000015.8:g.72270257G>C NCBI36
NG_009207.1:g.23168C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395105.9:c.904C>G MANE Select ENSP00000378537.4:p.Leu302Val
ENST00000323940.9:c.904C>G ENSP00000326085.5:p.Leu302Val
ENST00000395105.8:c.904C>G ENSP00000378537.4:p.Leu302Val
ENST00000416286.7:c.880C>G ENSP00000400403.3:p.Leu294Val
ENST00000423167.6:c.877C>G ENSP00000413012.2:p.Leu293Val
ENST00000449139.6:c.904C>G ENSP00000410221.2:p.Leu302Val
ENST00000535552.5:c.1015C>G ENSP00000440238.1:p.Leu339Val
ENST00000545137.5:n.613C>G
ENST00000563965.5:c.1021C>G ENSP00000456609.1:p.Leu341Val
ENST00000569936.5:c.1034C>G ENSP00000461799.1:p.Thr345Ser
ENST00000574278.5:c.949C>G ENSP00000458827.1:p.Leu317Val
ENST00000574439.5:n.1176C>G
ENST00000616000.4:c.904C>G ENSP00000479112.1:p.Leu302Val
NM_001142617.1:c.904C>G NP_001136089.1:p.Leu302Val
NM_001142618.1:c.904C>G NP_001136090.1:p.Leu302Val
NM_001142619.1:c.877C>G NP_001136091.1:p.Leu293Val
NM_001199040.1:c.1015C>G NP_001185969.1:p.Leu339Val
NM_001199041.1:c.949C>G NP_001185970.1:p.Leu317Val
NM_001199042.1:c.1021C>G NP_001185971.1:p.Leu341Val
NM_022369.3:c.904C>G NP_071764.3:p.Leu302Val
XM_011521883.1:c.904C>G XP_011520185.1:p.Leu302Val
XM_011521884.1:c.715C>G XP_011520186.1:p.Leu239Val
XM_011521885.1:c.1021C>G XP_011520187.1:p.Leu341Val
XR_931877.1:n.1027C>G
XM_011521885.2:c.1021C>G XP_011520187.1:p.Leu341Val
XM_017022478.1:c.952C>G XP_016877967.1:p.Leu318Val
XM_017022479.1:c.904C>G XP_016877968.1:p.Leu302Val
XM_017022480.1:c.715C>G XP_016877969.1:p.Leu239Val
XR_931877.2:n.1027C>G
NM_022369.4:c.904C>G MANE Select NP_071764.3:p.Leu302Val
NM_001142617.2:c.904C>G NP_001136089.1:p.Leu302Val
NM_001142619.2:c.877C>G NP_001136091.1:p.Leu293Val
NM_001199042.2:c.1021C>G NP_001185971.1:p.Leu341Val
NM_001142618.2:c.904C>G NP_001136090.1:p.Leu302Val
NM_001199040.2:c.1015C>G NP_001185969.1:p.Leu339Val
NM_001199041.2:c.949C>G NP_001185970.1:p.Leu317Val