Canonical Allele Identifier: CA393138888

Gene: STRA6

Linked Data

• gnomAD v4: 15-74196049-T-A
• MyVariant Identifiers: chr15:g.74488390T>A (hg19) ; chr15:g.74196049T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74196049T>A , CM000677.2:g.74196049T>A	GRCh38
NC_000015.9:g.74488390T>A , CM000677.1:g.74488390T>A	GRCh37
NC_000015.8:g.72275443T>A	NCBI36
NG_009207.1:g.17982A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.365A>T MANE Select	ENSP00000378537.4:p.Asp122Val
ENST00000323940.9:c.365A>T	ENSP00000326085.5:p.Asp122Val
ENST00000395105.8:c.365A>T	ENSP00000378537.4:p.Asp122Val
ENST00000416286.7:c.365A>T	ENSP00000400403.3:p.Asp122Val
ENST00000423167.6:c.338A>T	ENSP00000413012.2:p.Asp113Val
ENST00000432245.6:c.365A>T	ENSP00000407176.2:p.Asp122Val
ENST00000449139.6:c.365A>T	ENSP00000410221.2:p.Asp122Val
ENST00000535552.5:c.476A>T	ENSP00000440238.1:p.Asp159Val
ENST00000545137.5:n.241A>T
ENST00000563965.5:c.482A>T	ENSP00000456609.1:p.Asp161Val
ENST00000569936.5:c.365A>T	ENSP00000461799.1:p.Asp122Val
ENST00000573214.5:n.445A>T
ENST00000573456.5:n.649A>T
ENST00000573724.1:n.252-374A>T
ENST00000574278.5:c.410A>T	ENSP00000458827.1:p.Asp137Val
ENST00000574439.5:n.637A>T
ENST00000616000.4:c.365A>T	ENSP00000479112.1:p.Asp122Val
NM_001142617.1:c.365A>T	NP_001136089.1:p.Asp122Val
NM_001142618.1:c.365A>T	NP_001136090.1:p.Asp122Val
NM_001142619.1:c.338A>T	NP_001136091.1:p.Asp113Val
NM_001142620.1:c.365A>T	NP_001136092.1:p.Asp122Val
NM_001199040.1:c.476A>T	NP_001185969.1:p.Asp159Val
NM_001199041.1:c.410A>T	NP_001185970.1:p.Asp137Val
NM_001199042.1:c.482A>T	NP_001185971.1:p.Asp161Val
NM_022369.3:c.365A>T	NP_071764.3:p.Asp122Val
XM_011521883.1:c.365A>T	XP_011520185.1:p.Asp122Val
XM_011521884.1:c.176A>T	XP_011520186.1:p.Asp59Val
XM_011521885.1:c.482A>T	XP_011520187.1:p.Asp161Val
XR_931877.1:n.488A>T
XM_011521885.2:c.482A>T	XP_011520187.1:p.Asp161Val
XM_017022478.1:c.413A>T	XP_016877967.1:p.Asp138Val
XM_017022479.1:c.365A>T	XP_016877968.1:p.Asp122Val
XM_017022480.1:c.176A>T	XP_016877969.1:p.Asp59Val
XR_931877.2:n.488A>T
NM_022369.4:c.365A>T MANE Select	NP_071764.3:p.Asp122Val
NM_001142617.2:c.365A>T	NP_001136089.1:p.Asp122Val
NM_001142619.2:c.338A>T	NP_001136091.1:p.Asp113Val
NM_001199042.2:c.482A>T	NP_001185971.1:p.Asp161Val
NM_001142618.2:c.365A>T	NP_001136090.1:p.Asp122Val
NM_001142620.2:c.365A>T	NP_001136092.1:p.Asp122Val
NM_001199040.2:c.476A>T	NP_001185969.1:p.Asp159Val
NM_001199041.2:c.410A>T	NP_001185970.1:p.Asp137Val