Canonical Allele Identifier: CA491170328

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472510_74472511insACTATTG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180169_74180170insACTATTG , CM000677.2:g.74180169_74180170insACTATTG	GRCh38
NC_000015.9:g.74472510_74472511insACTATTG , CM000677.1:g.74472510_74472511insACTATTG	GRCh37
NC_000015.8:g.72259563_72259564insACTATTG	NCBI36
NG_009207.1:g.33861_33862insCAATAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1914_1915insCAATAGT MANE Select	ENSP00000378537.4:p.Trp639GlnfsTer2
ENST00000323940.9:c.1914_1915insCAATAGT	ENSP00000326085.5:p.Trp639GlnfsTer2
ENST00000395105.8:c.1914_1915insCAATAGT	ENSP00000378537.4:p.Trp639GlnfsTer2
ENST00000416286.7:c.1890_1891insCAATAGT	ENSP00000400403.3:p.Trp631GlnfsTer2
ENST00000423167.6:c.1887_1888insCAATAGT	ENSP00000413012.2:p.Trp630GlnfsTer2
ENST00000449139.6:c.1914_1915insCAATAGT	ENSP00000410221.2:p.Trp639GlnfsTer2
ENST00000535552.5:c.2025_2026insCAATAGT	ENSP00000440238.1:p.Trp676GlnfsTer2
ENST00000545137.5:n.1623_1624insCAATAGT
ENST00000563965.5:c.2031_2032insCAATAGT	ENSP00000456609.1:p.Trp678GlnfsTer2
ENST00000572785.1:c.769_770insCAATAGT
ENST00000574278.5:c.1959_1960insCAATAGT	ENSP00000458827.1:p.Trp654GlnfsTer2
ENST00000574439.5:n.2186_2187insCAATAGT
ENST00000616000.4:c.1914_1915insCAATAGT	ENSP00000479112.1:p.Trp639GlnfsTer2
NM_001142617.1:c.1914_1915insCAATAGT	NP_001136089.1:p.Trp639GlnfsTer2
NM_001142618.1:c.1914_1915insCAATAGT	NP_001136090.1:p.Trp639GlnfsTer2
NM_001142619.1:c.1887_1888insCAATAGT	NP_001136091.1:p.Trp630GlnfsTer2
NM_001199040.1:c.2025_2026insCAATAGT	NP_001185969.1:p.Trp676GlnfsTer2
NM_001199041.1:c.1959_1960insCAATAGT	NP_001185970.1:p.Trp654GlnfsTer2
NM_001199042.1:c.2031_2032insCAATAGT	NP_001185971.1:p.Trp678GlnfsTer2
NM_022369.3:c.1914_1915insCAATAGT	NP_071764.3:p.Trp639GlnfsTer2
XM_011521883.1:c.1914_1915insCAATAGT	XP_011520185.1:p.Trp639GlnfsTer2
XM_011521884.1:c.1725_1726insCAATAGT	XP_011520186.1:p.Trp576GlnfsTer2
XM_017022478.1:c.1962_1963insCAATAGT	XP_016877967.1:p.Trp655GlnfsTer2
XM_017022479.1:c.1914_1915insCAATAGT	XP_016877968.1:p.Trp639GlnfsTer2
XM_017022480.1:c.1725_1726insCAATAGT	XP_016877969.1:p.Trp576GlnfsTer2
NM_022369.4:c.1914_1915insCAATAGT MANE Select	NP_071764.3:p.Trp639GlnfsTer2
NM_001142617.2:c.1914_1915insCAATAGT	NP_001136089.1:p.Trp639GlnfsTer2
NM_001142619.2:c.1887_1888insCAATAGT	NP_001136091.1:p.Trp630GlnfsTer2
NM_001199042.2:c.2031_2032insCAATAGT	NP_001185971.1:p.Trp678GlnfsTer2
NM_001142618.2:c.1914_1915insCAATAGT	NP_001136090.1:p.Trp639GlnfsTer2
NM_001199040.2:c.2025_2026insCAATAGT	NP_001185969.1:p.Trp676GlnfsTer2
NM_001199041.2:c.1959_1960insCAATAGT	NP_001185970.1:p.Trp654GlnfsTer2