Canonical Allele Identifier: CA491173210

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74483202C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190861C>A , CM000677.2:g.74190861C>A	GRCh38
NC_000015.9:g.74483202C>A , CM000677.1:g.74483202C>A	GRCh37
NC_000015.8:g.72270255C>A	NCBI36
NG_009207.1:g.23170G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.906G>T MANE Select	ENSP00000378537.4:p.Leu302=
ENST00000323940.9:c.906G>T	ENSP00000326085.5:p.Leu302=
ENST00000395105.8:c.906G>T	ENSP00000378537.4:p.Leu302=
ENST00000416286.7:c.882G>T	ENSP00000400403.3:p.Leu294=
ENST00000423167.6:c.879G>T	ENSP00000413012.2:p.Leu293=
ENST00000449139.6:c.906G>T	ENSP00000410221.2:p.Leu302=
ENST00000535552.5:c.1017G>T	ENSP00000440238.1:p.Leu339=
ENST00000545137.5:n.615G>T
ENST00000563965.5:c.1023G>T	ENSP00000456609.1:p.Leu341=
ENST00000569936.5:c.1036G>T	ENSP00000461799.1:p.Asp346Tyr
ENST00000574278.5:c.951G>T	ENSP00000458827.1:p.Leu317=
ENST00000574439.5:n.1178G>T
ENST00000616000.4:c.906G>T	ENSP00000479112.1:p.Leu302=
NM_001142617.1:c.906G>T	NP_001136089.1:p.Leu302=
NM_001142618.1:c.906G>T	NP_001136090.1:p.Leu302=
NM_001142619.1:c.879G>T	NP_001136091.1:p.Leu293=
NM_001199040.1:c.1017G>T	NP_001185969.1:p.Leu339=
NM_001199041.1:c.951G>T	NP_001185970.1:p.Leu317=
NM_001199042.1:c.1023G>T	NP_001185971.1:p.Leu341=
NM_022369.3:c.906G>T	NP_071764.3:p.Leu302=
XM_011521883.1:c.906G>T	XP_011520185.1:p.Leu302=
XM_011521884.1:c.717G>T	XP_011520186.1:p.Leu239=
XM_011521885.1:c.1023G>T	XP_011520187.1:p.Leu341=
XR_931877.1:n.1029G>T
XM_011521885.2:c.1023G>T	XP_011520187.1:p.Leu341=
XM_017022478.1:c.954G>T	XP_016877967.1:p.Leu318=
XM_017022479.1:c.906G>T	XP_016877968.1:p.Leu302=
XM_017022480.1:c.717G>T	XP_016877969.1:p.Leu239=
XR_931877.2:n.1029G>T
NM_022369.4:c.906G>T MANE Select	NP_071764.3:p.Leu302=
NM_001142617.2:c.906G>T	NP_001136089.1:p.Leu302=
NM_001142619.2:c.879G>T	NP_001136091.1:p.Leu293=
NM_001199042.2:c.1023G>T	NP_001185971.1:p.Leu341=
NM_001142618.2:c.906G>T	NP_001136090.1:p.Leu302=
NM_001199040.2:c.1017G>T	NP_001185969.1:p.Leu339=
NM_001199041.2:c.951G>T	NP_001185970.1:p.Leu317=