Canonical Allele Identifier: CA393135322

Gene: STRA6

Linked Data

• gnomAD v4: 15-74190859-G-C
• MyVariant Identifiers: chr15:g.74483200G>C (hg19) ; chr15:g.74190859G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190859G>C , CM000677.2:g.74190859G>C	GRCh38
NC_000015.9:g.74483200G>C , CM000677.1:g.74483200G>C	GRCh37
NC_000015.8:g.72270253G>C	NCBI36
NG_009207.1:g.23172C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.908C>G MANE Select	ENSP00000378537.4:p.Thr303Arg
ENST00000323940.9:c.908C>G	ENSP00000326085.5:p.Thr303Arg
ENST00000395105.8:c.908C>G	ENSP00000378537.4:p.Thr303Arg
ENST00000416286.7:c.884C>G	ENSP00000400403.3:p.Thr295Arg
ENST00000423167.6:c.881C>G	ENSP00000413012.2:p.Thr294Arg
ENST00000449139.6:c.908C>G	ENSP00000410221.2:p.Thr303Arg
ENST00000535552.5:c.1019C>G	ENSP00000440238.1:p.Thr340Arg
ENST00000545137.5:n.617C>G
ENST00000563965.5:c.1025C>G	ENSP00000456609.1:p.Thr342Arg
ENST00000569936.5:c.1038C>G	ENSP00000461799.1:p.Asp346Glu
ENST00000574278.5:c.953C>G	ENSP00000458827.1:p.Thr318Arg
ENST00000574439.5:n.1180C>G
ENST00000616000.4:c.908C>G	ENSP00000479112.1:p.Thr303Arg
NM_001142617.1:c.908C>G	NP_001136089.1:p.Thr303Arg
NM_001142618.1:c.908C>G	NP_001136090.1:p.Thr303Arg
NM_001142619.1:c.881C>G	NP_001136091.1:p.Thr294Arg
NM_001199040.1:c.1019C>G	NP_001185969.1:p.Thr340Arg
NM_001199041.1:c.953C>G	NP_001185970.1:p.Thr318Arg
NM_001199042.1:c.1025C>G	NP_001185971.1:p.Thr342Arg
NM_022369.3:c.908C>G	NP_071764.3:p.Thr303Arg
XM_011521883.1:c.908C>G	XP_011520185.1:p.Thr303Arg
XM_011521884.1:c.719C>G	XP_011520186.1:p.Thr240Arg
XM_011521885.1:c.1025C>G	XP_011520187.1:p.Thr342Arg
XR_931877.1:n.1031C>G
XM_011521885.2:c.1025C>G	XP_011520187.1:p.Thr342Arg
XM_017022478.1:c.956C>G	XP_016877967.1:p.Thr319Arg
XM_017022479.1:c.908C>G	XP_016877968.1:p.Thr303Arg
XM_017022480.1:c.719C>G	XP_016877969.1:p.Thr240Arg
XR_931877.2:n.1031C>G
NM_022369.4:c.908C>G MANE Select	NP_071764.3:p.Thr303Arg
NM_001142617.2:c.908C>G	NP_001136089.1:p.Thr303Arg
NM_001142619.2:c.881C>G	NP_001136091.1:p.Thr294Arg
NM_001199042.2:c.1025C>G	NP_001185971.1:p.Thr342Arg
NM_001142618.2:c.908C>G	NP_001136090.1:p.Thr303Arg
NM_001199040.2:c.1019C>G	NP_001185969.1:p.Thr340Arg
NM_001199041.2:c.953C>G	NP_001185970.1:p.Thr318Arg