Canonical Allele Identifier: CA2629451375

Gene: STRA6

Linked Data

• gnomAD v4: 15-74190865-G-GTAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190867_74190870dup , CM000677.2:g.74190867_74190870dup	GRCh38
NC_000015.9:g.74483208_74483211dup , CM000677.1:g.74483208_74483211dup	GRCh37
NC_000015.8:g.72270261_72270264dup	NCBI36
NG_009207.1:g.23162_23165dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.898_901dup MANE Select	ENSP00000378537.4:p.Thr301SerfsTer?
ENST00000323940.9:c.898_901dup	ENSP00000326085.5:p.Thr301SerfsTer?
ENST00000395105.8:c.898_901dup	ENSP00000378537.4:p.Thr301SerfsTer?
ENST00000416286.7:c.874_877dup	ENSP00000400403.3:p.Thr293SerfsTer?
ENST00000423167.6:c.871_874dup	ENSP00000413012.2:p.Thr292SerfsTer?
ENST00000449139.6:c.898_901dup	ENSP00000410221.2:p.Thr301SerfsTer?
ENST00000535552.5:c.1009_1012dup	ENSP00000440238.1:p.Thr338SerfsTer?
ENST00000545137.5:n.607_610dup
ENST00000563965.5:c.1015_1018dup	ENSP00000456609.1:p.Thr340SerfsTer?
ENST00000569936.5:c.1028_1031dup	ENSP00000461799.1:p.Tyr344Ter
ENST00000574278.5:c.943_946dup	ENSP00000458827.1:p.Thr316SerfsTer?
ENST00000574439.5:n.1170_1173dup
ENST00000616000.4:c.898_901dup	ENSP00000479112.1:p.Thr301SerfsTer?
NM_001142617.1:c.898_901dup	NP_001136089.1:p.Thr301SerfsTer?
NM_001142618.1:c.898_901dup	NP_001136090.1:p.Thr301SerfsTer?
NM_001142619.1:c.871_874dup	NP_001136091.1:p.Thr292SerfsTer?
NM_001199040.1:c.1009_1012dup	NP_001185969.1:p.Thr338SerfsTer?
NM_001199041.1:c.943_946dup	NP_001185970.1:p.Thr316SerfsTer?
NM_001199042.1:c.1015_1018dup	NP_001185971.1:p.Thr340SerfsTer?
NM_022369.3:c.898_901dup	NP_071764.3:p.Thr301SerfsTer?
XM_011521883.1:c.898_901dup	XP_011520185.1:p.Thr301SerfsTer?
XM_011521884.1:c.709_712dup	XP_011520186.1:p.Thr238SerfsTer?
XM_011521885.1:c.1015_1018dup	XP_011520187.1:p.Thr340SerfsTer?
XR_931877.1:n.1021_1024dup
XM_011521885.2:c.1015_1018dup	XP_011520187.1:p.Thr340SerfsTer?
XM_017022478.1:c.946_949dup	XP_016877967.1:p.Thr317SerfsTer?
XM_017022479.1:c.898_901dup	XP_016877968.1:p.Thr301SerfsTer?
XM_017022480.1:c.709_712dup	XP_016877969.1:p.Thr238SerfsTer?
XR_931877.2:n.1021_1024dup
NM_022369.4:c.898_901dup MANE Select	NP_071764.3:p.Thr301SerfsTer?
NM_001142617.2:c.898_901dup	NP_001136089.1:p.Thr301SerfsTer?
NM_001142619.2:c.871_874dup	NP_001136091.1:p.Thr292SerfsTer?
NM_001199042.2:c.1015_1018dup	NP_001185971.1:p.Thr340SerfsTer?
NM_001142618.2:c.898_901dup	NP_001136090.1:p.Thr301SerfsTer?
NM_001199040.2:c.1009_1012dup	NP_001185969.1:p.Thr338SerfsTer?
NM_001199041.2:c.943_946dup	NP_001185970.1:p.Thr316SerfsTer?