Canonical Allele Identifier: CA491173219

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74483208A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190867A>T , CM000677.2:g.74190867A>T	GRCh38
NC_000015.9:g.74483208A>T , CM000677.1:g.74483208A>T	GRCh37
NC_000015.8:g.72270261A>T	NCBI36
NG_009207.1:g.23164T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.900T>A MANE Select	ENSP00000378537.4:p.Ala300=
ENST00000323940.9:c.900T>A	ENSP00000326085.5:p.Ala300=
ENST00000395105.8:c.900T>A	ENSP00000378537.4:p.Ala300=
ENST00000416286.7:c.876T>A	ENSP00000400403.3:p.Ala292=
ENST00000423167.6:c.873T>A	ENSP00000413012.2:p.Ala291=
ENST00000449139.6:c.900T>A	ENSP00000410221.2:p.Ala300=
ENST00000535552.5:c.1011T>A	ENSP00000440238.1:p.Ala337=
ENST00000545137.5:n.609T>A
ENST00000563965.5:c.1017T>A	ENSP00000456609.1:p.Ala339=
ENST00000569936.5:c.1030T>A	ENSP00000461799.1:p.Tyr344Asn
ENST00000574278.5:c.945T>A	ENSP00000458827.1:p.Ala315=
ENST00000574439.5:n.1172T>A
ENST00000616000.4:c.900T>A	ENSP00000479112.1:p.Ala300=
NM_001142617.1:c.900T>A	NP_001136089.1:p.Ala300=
NM_001142618.1:c.900T>A	NP_001136090.1:p.Ala300=
NM_001142619.1:c.873T>A	NP_001136091.1:p.Ala291=
NM_001199040.1:c.1011T>A	NP_001185969.1:p.Ala337=
NM_001199041.1:c.945T>A	NP_001185970.1:p.Ala315=
NM_001199042.1:c.1017T>A	NP_001185971.1:p.Ala339=
NM_022369.3:c.900T>A	NP_071764.3:p.Ala300=
XM_011521883.1:c.900T>A	XP_011520185.1:p.Ala300=
XM_011521884.1:c.711T>A	XP_011520186.1:p.Ala237=
XM_011521885.1:c.1017T>A	XP_011520187.1:p.Ala339=
XR_931877.1:n.1023T>A
XM_011521885.2:c.1017T>A	XP_011520187.1:p.Ala339=
XM_017022478.1:c.948T>A	XP_016877967.1:p.Ala316=
XM_017022479.1:c.900T>A	XP_016877968.1:p.Ala300=
XM_017022480.1:c.711T>A	XP_016877969.1:p.Ala237=
XR_931877.2:n.1023T>A
NM_022369.4:c.900T>A MANE Select	NP_071764.3:p.Ala300=
NM_001142617.2:c.900T>A	NP_001136089.1:p.Ala300=
NM_001142619.2:c.873T>A	NP_001136091.1:p.Ala291=
NM_001199042.2:c.1017T>A	NP_001185971.1:p.Ala339=
NM_001142618.2:c.900T>A	NP_001136090.1:p.Ala300=
NM_001199040.2:c.1011T>A	NP_001185969.1:p.Ala337=
NM_001199041.2:c.945T>A	NP_001185970.1:p.Ala315=