Canonical Allele Identifier: CA393128227

Gene: STRA6

Linked Data

• gnomAD v4: 15-74180126-A-T
• MyVariant Identifiers: chr15:g.74472467A>T (hg19) ; chr15:g.74180126A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180126A>T , CM000677.2:g.74180126A>T	GRCh38
NC_000015.9:g.74472467A>T , CM000677.1:g.74472467A>T	GRCh37
NC_000015.8:g.72259520A>T	NCBI36
NG_009207.1:g.33905T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1958T>A MANE Select	ENSP00000378537.4:p.Val653Asp
ENST00000323940.9:c.1958T>A	ENSP00000326085.5:p.Val653Asp
ENST00000395105.8:c.1958T>A	ENSP00000378537.4:p.Val653Asp
ENST00000416286.7:c.1934T>A	ENSP00000400403.3:p.Val645Asp
ENST00000423167.6:c.1931T>A	ENSP00000413012.2:p.Val644Asp
ENST00000449139.6:c.1958T>A	ENSP00000410221.2:p.Val653Asp
ENST00000535552.5:c.2069T>A	ENSP00000440238.1:p.Val690Asp
ENST00000545137.5:n.1667T>A
ENST00000563965.5:c.2075T>A	ENSP00000456609.1:p.Val692Asp
ENST00000574278.5:c.2003T>A	ENSP00000458827.1:p.Val668Asp
ENST00000574439.5:n.2230T>A
ENST00000616000.4:c.1958T>A	ENSP00000479112.1:p.Val653Asp
NM_001142617.1:c.1958T>A	NP_001136089.1:p.Val653Asp
NM_001142618.1:c.1958T>A	NP_001136090.1:p.Val653Asp
NM_001142619.1:c.1931T>A	NP_001136091.1:p.Val644Asp
NM_001199040.1:c.2069T>A	NP_001185969.1:p.Val690Asp
NM_001199041.1:c.2003T>A	NP_001185970.1:p.Val668Asp
NM_001199042.1:c.2075T>A	NP_001185971.1:p.Val692Asp
NM_022369.3:c.1958T>A	NP_071764.3:p.Val653Asp
XM_011521883.1:c.1958T>A	XP_011520185.1:p.Val653Asp
XM_011521884.1:c.1769T>A	XP_011520186.1:p.Val590Asp
XM_017022478.1:c.2006T>A	XP_016877967.1:p.Val669Asp
XM_017022479.1:c.1958T>A	XP_016877968.1:p.Val653Asp
XM_017022480.1:c.1769T>A	XP_016877969.1:p.Val590Asp
NM_022369.4:c.1958T>A MANE Select	NP_071764.3:p.Val653Asp
NM_001142617.2:c.1958T>A	NP_001136089.1:p.Val653Asp
NM_001142619.2:c.1931T>A	NP_001136091.1:p.Val644Asp
NM_001199042.2:c.2075T>A	NP_001185971.1:p.Val692Asp
NM_001142618.2:c.1958T>A	NP_001136090.1:p.Val653Asp
NM_001199040.2:c.2069T>A	NP_001185969.1:p.Val690Asp
NM_001199041.2:c.2003T>A	NP_001185970.1:p.Val668Asp