Canonical Allele Identifier: CA393128169

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472436A>T (hg19) ; chr15:g.74180095A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180095A>T , CM000677.2:g.74180095A>T	GRCh38
NC_000015.9:g.74472436A>T , CM000677.1:g.74472436A>T	GRCh37
NC_000015.8:g.72259489A>T	NCBI36
NG_009207.1:g.33936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1989T>A MANE Select	ENSP00000378537.4:p.Asn663Lys
ENST00000323940.9:c.1989T>A	ENSP00000326085.5:p.Asn663Lys
ENST00000395105.8:c.1989T>A	ENSP00000378537.4:p.Asn663Lys
ENST00000416286.7:c.1965T>A	ENSP00000400403.3:p.Asn655Lys
ENST00000423167.6:c.1962T>A	ENSP00000413012.2:p.Asn654Lys
ENST00000449139.6:c.1989T>A	ENSP00000410221.2:p.Asn663Lys
ENST00000535552.5:c.2100T>A	ENSP00000440238.1:p.Asn700Lys
ENST00000545137.5:n.1698T>A
ENST00000563965.5:c.2106T>A	ENSP00000456609.1:p.Asn702Lys
ENST00000574278.5:c.2034T>A	ENSP00000458827.1:p.Asn678Lys
ENST00000574439.5:n.2261T>A
ENST00000616000.4:c.1989T>A	ENSP00000479112.1:p.Asn663Lys
NM_001142617.1:c.1989T>A	NP_001136089.1:p.Asn663Lys
NM_001142618.1:c.1989T>A	NP_001136090.1:p.Asn663Lys
NM_001142619.1:c.1962T>A	NP_001136091.1:p.Asn654Lys
NM_001199040.1:c.2100T>A	NP_001185969.1:p.Asn700Lys
NM_001199041.1:c.2034T>A	NP_001185970.1:p.Asn678Lys
NM_001199042.1:c.2106T>A	NP_001185971.1:p.Asn702Lys
NM_022369.3:c.1989T>A	NP_071764.3:p.Asn663Lys
XM_011521883.1:c.1989T>A	XP_011520185.1:p.Asn663Lys
XM_011521884.1:c.1800T>A	XP_011520186.1:p.Asn600Lys
XM_017022478.1:c.2037T>A	XP_016877967.1:p.Asn679Lys
XM_017022479.1:c.1989T>A	XP_016877968.1:p.Asn663Lys
XM_017022480.1:c.1800T>A	XP_016877969.1:p.Asn600Lys
NM_022369.4:c.1989T>A MANE Select	NP_071764.3:p.Asn663Lys
NM_001142617.2:c.1989T>A	NP_001136089.1:p.Asn663Lys
NM_001142619.2:c.1962T>A	NP_001136091.1:p.Asn654Lys
NM_001199042.2:c.2106T>A	NP_001185971.1:p.Asn702Lys
NM_001142618.2:c.1989T>A	NP_001136090.1:p.Asn663Lys
NM_001199040.2:c.2100T>A	NP_001185969.1:p.Asn700Lys
NM_001199041.2:c.2034T>A	NP_001185970.1:p.Asn678Lys