Canonical Allele Identifier: CA491170331

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472513_74472514insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180172_74180173insT , CM000677.2:g.74180172_74180173insT	GRCh38
NC_000015.9:g.74472513_74472514insT , CM000677.1:g.74472513_74472514insT	GRCh37
NC_000015.8:g.72259566_72259567insT	NCBI36
NG_009207.1:g.33858_33859insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1911_1912insA MANE Select	ENSP00000378537.4:p.Arg638ThrfsTer?
ENST00000323940.9:c.1911_1912insA	ENSP00000326085.5:p.Arg638ThrfsTer?
ENST00000395105.8:c.1911_1912insA	ENSP00000378537.4:p.Arg638ThrfsTer?
ENST00000416286.7:c.1887_1888insA	ENSP00000400403.3:p.Arg630ThrfsTer?
ENST00000423167.6:c.1884_1885insA	ENSP00000413012.2:p.Arg629ThrfsTer?
ENST00000449139.6:c.1911_1912insA	ENSP00000410221.2:p.Arg638ThrfsTer?
ENST00000535552.5:c.2022_2023insA	ENSP00000440238.1:p.Arg675ThrfsTer?
ENST00000545137.5:n.1620_1621insA
ENST00000563965.5:c.2028_2029insA	ENSP00000456609.1:p.Arg677ThrfsTer?
ENST00000572785.1:c.766_767insA
ENST00000574278.5:c.1956_1957insA	ENSP00000458827.1:p.Arg653ThrfsTer?
ENST00000574439.5:n.2183_2184insA
ENST00000616000.4:c.1911_1912insA	ENSP00000479112.1:p.Arg638ThrfsTer?
NM_001142617.1:c.1911_1912insA	NP_001136089.1:p.Arg638ThrfsTer?
NM_001142618.1:c.1911_1912insA	NP_001136090.1:p.Arg638ThrfsTer?
NM_001142619.1:c.1884_1885insA	NP_001136091.1:p.Arg629ThrfsTer?
NM_001199040.1:c.2022_2023insA	NP_001185969.1:p.Arg675ThrfsTer?
NM_001199041.1:c.1956_1957insA	NP_001185970.1:p.Arg653ThrfsTer?
NM_001199042.1:c.2028_2029insA	NP_001185971.1:p.Arg677ThrfsTer?
NM_022369.3:c.1911_1912insA	NP_071764.3:p.Arg638ThrfsTer?
XM_011521883.1:c.1911_1912insA	XP_011520185.1:p.Arg638ThrfsTer?
XM_011521884.1:c.1722_1723insA	XP_011520186.1:p.Arg575ThrfsTer?
XM_017022478.1:c.1959_1960insA	XP_016877967.1:p.Arg654ThrfsTer?
XM_017022479.1:c.1911_1912insA	XP_016877968.1:p.Arg638ThrfsTer?
XM_017022480.1:c.1722_1723insA	XP_016877969.1:p.Arg575ThrfsTer?
NM_022369.4:c.1911_1912insA MANE Select	NP_071764.3:p.Arg638ThrfsTer?
NM_001142617.2:c.1911_1912insA	NP_001136089.1:p.Arg638ThrfsTer?
NM_001142619.2:c.1884_1885insA	NP_001136091.1:p.Arg629ThrfsTer?
NM_001199042.2:c.2028_2029insA	NP_001185971.1:p.Arg677ThrfsTer?
NM_001142618.2:c.1911_1912insA	NP_001136090.1:p.Arg638ThrfsTer?
NM_001199040.2:c.2022_2023insA	NP_001185969.1:p.Arg675ThrfsTer?
NM_001199041.2:c.1956_1957insA	NP_001185970.1:p.Arg653ThrfsTer?