Canonical Allele Identifier: CA393135334
Gene: STRA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74190866T>A , CM000677.2:g.74190866T>A GRCh38
NC_000015.9:g.74483207T>A , CM000677.1:g.74483207T>A GRCh37
NC_000015.8:g.72270260T>A NCBI36
NG_009207.1:g.23165A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395105.9:c.901A>T MANE Select ENSP00000378537.4:p.Thr301Ser
ENST00000323940.9:c.901A>T ENSP00000326085.5:p.Thr301Ser
ENST00000395105.8:c.901A>T ENSP00000378537.4:p.Thr301Ser
ENST00000416286.7:c.877A>T ENSP00000400403.3:p.Thr293Ser
ENST00000423167.6:c.874A>T ENSP00000413012.2:p.Thr292Ser
ENST00000449139.6:c.901A>T ENSP00000410221.2:p.Thr301Ser
ENST00000535552.5:c.1012A>T ENSP00000440238.1:p.Thr338Ser
ENST00000545137.5:n.610A>T
ENST00000563965.5:c.1018A>T ENSP00000456609.1:p.Thr340Ser
ENST00000569936.5:c.1031A>T ENSP00000461799.1:p.Tyr344Phe
ENST00000574278.5:c.946A>T ENSP00000458827.1:p.Thr316Ser
ENST00000574439.5:n.1173A>T
ENST00000616000.4:c.901A>T ENSP00000479112.1:p.Thr301Ser
NM_001142617.1:c.901A>T NP_001136089.1:p.Thr301Ser
NM_001142618.1:c.901A>T NP_001136090.1:p.Thr301Ser
NM_001142619.1:c.874A>T NP_001136091.1:p.Thr292Ser
NM_001199040.1:c.1012A>T NP_001185969.1:p.Thr338Ser
NM_001199041.1:c.946A>T NP_001185970.1:p.Thr316Ser
NM_001199042.1:c.1018A>T NP_001185971.1:p.Thr340Ser
NM_022369.3:c.901A>T NP_071764.3:p.Thr301Ser
XM_011521883.1:c.901A>T XP_011520185.1:p.Thr301Ser
XM_011521884.1:c.712A>T XP_011520186.1:p.Thr238Ser
XM_011521885.1:c.1018A>T XP_011520187.1:p.Thr340Ser
XR_931877.1:n.1024A>T
XM_011521885.2:c.1018A>T XP_011520187.1:p.Thr340Ser
XM_017022478.1:c.949A>T XP_016877967.1:p.Thr317Ser
XM_017022479.1:c.901A>T XP_016877968.1:p.Thr301Ser
XM_017022480.1:c.712A>T XP_016877969.1:p.Thr238Ser
XR_931877.2:n.1024A>T
NM_022369.4:c.901A>T MANE Select NP_071764.3:p.Thr301Ser
NM_001142617.2:c.901A>T NP_001136089.1:p.Thr301Ser
NM_001142619.2:c.874A>T NP_001136091.1:p.Thr292Ser
NM_001199042.2:c.1018A>T NP_001185971.1:p.Thr340Ser
NM_001142618.2:c.901A>T NP_001136090.1:p.Thr301Ser
NM_001199040.2:c.1012A>T NP_001185969.1:p.Thr338Ser
NM_001199041.2:c.946A>T NP_001185970.1:p.Thr316Ser