Canonical Allele Identifier: CA2629451334

Gene: STRA6

Linked Data

• gnomAD v4: 15-74190817-GCAGTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190821_74190825del , CM000677.2:g.74190821_74190825del	GRCh38
NC_000015.9:g.74483162_74483166del , CM000677.1:g.74483162_74483166del	GRCh37
NC_000015.8:g.72270215_72270219del	NCBI36
NG_009207.1:g.23209_23213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.927+18_927+22del MANE Select	ENSP00000378537.4:n.927+18_927+22del
ENST00000323940.9:c.927+18_927+22del	ENSP00000326085.5:n.927+18_927+22del
ENST00000395105.8:c.927+18_927+22del	ENSP00000378537.4:n.927+18_927+22del
ENST00000416286.7:c.903+18_903+22del	ENSP00000400403.3:n.903+18_903+22del
ENST00000423167.6:c.900+18_900+22del	ENSP00000413012.2:n.900+18_900+22del
ENST00000449139.6:c.927+18_927+22del	ENSP00000410221.2:n.927+18_927+22del
ENST00000535552.5:c.1038+18_1038+22del	ENSP00000440238.1:n.1038+18_1038+22del
ENST00000545137.5:n.636+18_636+22del
ENST00000563965.5:c.1044+18_1044+22del	ENSP00000456609.1:n.1044+18_1044+22del
ENST00000569936.5:c.1057+18_1057+22del	ENSP00000461799.1:n.1057+18_1057+22del
ENST00000574278.5:c.972+18_972+22del	ENSP00000458827.1:n.972+18_972+22del
ENST00000574439.5:n.1199+18_1199+22del
ENST00000616000.4:c.927+18_927+22del	ENSP00000479112.1:n.927+18_927+22del
NM_001142617.1:c.927+18_927+22del	NP_001136089.1:n.927+18_927+22del
NM_001142618.1:c.927+18_927+22del	NP_001136090.1:n.927+18_927+22del
NM_001142619.1:c.900+18_900+22del	NP_001136091.1:n.900+18_900+22del
NM_001199040.1:c.1038+18_1038+22del	NP_001185969.1:n.1038+18_1038+22del
NM_001199041.1:c.972+18_972+22del	NP_001185970.1:n.972+18_972+22del
NM_001199042.1:c.1044+18_1044+22del	NP_001185971.1:n.1044+18_1044+22del
NM_022369.3:c.927+18_927+22del	NP_071764.3:n.927+18_927+22del
XM_011521883.1:c.927+18_927+22del	XP_011520185.1:n.927+18_927+22del
XM_011521884.1:c.738+18_738+22del	XP_011520186.1:n.738+18_738+22del
XM_011521885.1:c.1044+18_1044+22del	XP_011520187.1:n.1044+18_1044+22del
XR_931877.1:n.1050+18_1050+22del
XM_011521885.2:c.1044+18_1044+22del	XP_011520187.1:n.1044+18_1044+22del
XM_017022478.1:c.975+18_975+22del	XP_016877967.1:n.975+18_975+22del
XM_017022479.1:c.927+18_927+22del	XP_016877968.1:n.927+18_927+22del
XM_017022480.1:c.738+18_738+22del	XP_016877969.1:n.738+18_738+22del
XR_931877.2:n.1050+18_1050+22del
NM_022369.4:c.927+18_927+22del MANE Select	NP_071764.3:n.927+18_927+22del
NM_001142617.2:c.927+18_927+22del	NP_001136089.1:n.927+18_927+22del
NM_001142619.2:c.900+18_900+22del	NP_001136091.1:n.900+18_900+22del
NM_001199042.2:c.1044+18_1044+22del	NP_001185971.1:n.1044+18_1044+22del
NM_001142618.2:c.927+18_927+22del	NP_001136090.1:n.927+18_927+22del
NM_001199040.2:c.1038+18_1038+22del	NP_001185969.1:n.1038+18_1038+22del
NM_001199041.2:c.972+18_972+22del	NP_001185970.1:n.972+18_972+22del