Canonical Allele Identifier: CA2187549725

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180163G= , CM000677.2:g.74180163G=	GRCh38
NC_000015.9:g.74472504G= , CM000677.1:g.74472504G=	GRCh37
NC_000015.8:g.72259557G=	NCBI36
NG_009207.1:g.33868C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1921C= MANE Select	ENSP00000378537.4:p.Leu641=
ENST00000323940.9:c.1921C=	ENSP00000326085.5:p.Leu641=
ENST00000395105.8:c.1921C=	ENSP00000378537.4:p.Leu641=
ENST00000416286.7:c.1897C=	ENSP00000400403.3:p.Leu633=
ENST00000423167.6:c.1894C=	ENSP00000413012.2:p.Leu632=
ENST00000449139.6:c.1921C=	ENSP00000410221.2:p.Leu641=
ENST00000535552.5:c.2032C=	ENSP00000440238.1:p.Leu678=
ENST00000545137.5:n.1630C=
ENST00000563965.5:c.2038C=	ENSP00000456609.1:p.Leu680=
ENST00000572785.1:c.776C=
ENST00000574278.5:c.1966C=	ENSP00000458827.1:p.Leu656=
ENST00000574439.5:n.2193C=
ENST00000616000.4:c.1921C=	ENSP00000479112.1:p.Leu641=
NM_001142617.1:c.1921C=	NP_001136089.1:p.Leu641=
NM_001142618.1:c.1921C=	NP_001136090.1:p.Leu641=
NM_001142619.1:c.1894C=	NP_001136091.1:p.Leu632=
NM_001199040.1:c.2032C=	NP_001185969.1:p.Leu678=
NM_001199041.1:c.1966C=	NP_001185970.1:p.Leu656=
NM_001199042.1:c.2038C=	NP_001185971.1:p.Leu680=
NM_022369.3:c.1921C=	NP_071764.3:p.Leu641=
XM_011521883.1:c.1921C=	XP_011520185.1:p.Leu641=
XM_011521884.1:c.1732C=	XP_011520186.1:p.Leu578=
XM_017022478.1:c.1969C=	XP_016877967.1:p.Leu657=
XM_017022479.1:c.1921C=	XP_016877968.1:p.Leu641=
XM_017022480.1:c.1732C=	XP_016877969.1:p.Leu578=
NM_022369.4:c.1921C= MANE Select	NP_071764.3:p.Leu641=
NM_001142617.2:c.1921C=	NP_001136089.1:p.Leu641=
NM_001142619.2:c.1894C=	NP_001136091.1:p.Leu632=
NM_001199042.2:c.2038C=	NP_001185971.1:p.Leu680=
NM_001142618.2:c.1921C=	NP_001136090.1:p.Leu641=
NM_001199040.2:c.2032C=	NP_001185969.1:p.Leu678=
NM_001199041.2:c.1966C=	NP_001185970.1:p.Leu656=