Canonical Allele Identifier: CA619110260

Gene: STRA6

Linked Data

• dbSNP Id: rs1234502781
• gnomAD v2: 15-74483103-TG-T
• gnomAD v3: 15-74190762-TG-T
• gnomAD v4: 15-74190762-TG-T
• MyVariant Identifiers: chr15:g.74483104del (hg19) ; chr15:g.74190763del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190765del , CM000677.2:g.74190765del	GRCh38
NC_000015.9:g.74483106del , CM000677.1:g.74483106del	GRCh37
NC_000015.8:g.72270159del	NCBI36
NG_009207.1:g.23268del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.927+77del MANE Select	ENSP00000378537.4:n.927+77del
ENST00000323940.9:c.927+77del	ENSP00000326085.5:n.927+77del
ENST00000395105.8:c.927+77del	ENSP00000378537.4:n.927+77del
ENST00000416286.7:c.903+77del	ENSP00000400403.3:n.903+77del
ENST00000423167.6:c.900+77del	ENSP00000413012.2:n.900+77del
ENST00000449139.6:c.927+77del	ENSP00000410221.2:n.927+77del
ENST00000535552.5:c.1038+77del	ENSP00000440238.1:n.1038+77del
ENST00000545137.5:n.636+77del
ENST00000563965.5:c.1044+77del	ENSP00000456609.1:n.1044+77del
ENST00000569936.5:c.1057+77del	ENSP00000461799.1:n.1057+77del
ENST00000574278.5:c.972+77del	ENSP00000458827.1:n.972+77del
ENST00000574439.5:n.1199+77del
ENST00000616000.4:c.927+77del	ENSP00000479112.1:n.927+77del
NM_001142617.1:c.927+77del	NP_001136089.1:n.927+77del
NM_001142618.1:c.927+77del	NP_001136090.1:n.927+77del
NM_001142619.1:c.900+77del	NP_001136091.1:n.900+77del
NM_001199040.1:c.1038+77del	NP_001185969.1:n.1038+77del
NM_001199041.1:c.972+77del	NP_001185970.1:n.972+77del
NM_001199042.1:c.1044+77del	NP_001185971.1:n.1044+77del
NM_022369.3:c.927+77del	NP_071764.3:n.927+77del
XM_011521883.1:c.927+77del	XP_011520185.1:n.927+77del
XM_011521884.1:c.738+77del	XP_011520186.1:n.738+77del
XM_011521885.1:c.1044+77del	XP_011520187.1:n.1044+77del
XR_931877.1:n.1050+77del
XM_011521885.2:c.1044+77del	XP_011520187.1:n.1044+77del
XM_017022478.1:c.975+77del	XP_016877967.1:n.975+77del
XM_017022479.1:c.927+77del	XP_016877968.1:n.927+77del
XM_017022480.1:c.738+77del	XP_016877969.1:n.738+77del
XR_931877.2:n.1050+77del
NM_022369.4:c.927+77del MANE Select	NP_071764.3:n.927+77del
NM_001142617.2:c.927+77del	NP_001136089.1:n.927+77del
NM_001142619.2:c.900+77del	NP_001136091.1:n.900+77del
NM_001199042.2:c.1044+77del	NP_001185971.1:n.1044+77del
NM_001142618.2:c.927+77del	NP_001136090.1:n.927+77del
NM_001199040.2:c.1038+77del	NP_001185969.1:n.1038+77del
NM_001199041.2:c.972+77del	NP_001185970.1:n.972+77del