Canonical Allele Identifier: CA2187549693

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180098G= , CM000677.2:g.74180098G=	GRCh38
NC_000015.9:g.74472439G= , CM000677.1:g.74472439G=	GRCh37
NC_000015.8:g.72259492G=	NCBI36
NG_009207.1:g.33933C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1986C= MANE Select	ENSP00000378537.4:p.Ala662=
ENST00000323940.9:c.1986C=	ENSP00000326085.5:p.Ala662=
ENST00000395105.8:c.1986C=	ENSP00000378537.4:p.Ala662=
ENST00000416286.7:c.1962C=	ENSP00000400403.3:p.Ala654=
ENST00000423167.6:c.1959C=	ENSP00000413012.2:p.Ala653=
ENST00000449139.6:c.1986C=	ENSP00000410221.2:p.Ala662=
ENST00000535552.5:c.2097C=	ENSP00000440238.1:p.Ala699=
ENST00000545137.5:n.1695C=
ENST00000563965.5:c.2103C=	ENSP00000456609.1:p.Ala701=
ENST00000574278.5:c.2031C=	ENSP00000458827.1:p.Ala677=
ENST00000574439.5:n.2258C=
ENST00000616000.4:c.1986C=	ENSP00000479112.1:p.Ala662=
NM_001142617.1:c.1986C=	NP_001136089.1:p.Ala662=
NM_001142618.1:c.1986C=	NP_001136090.1:p.Ala662=
NM_001142619.1:c.1959C=	NP_001136091.1:p.Ala653=
NM_001199040.1:c.2097C=	NP_001185969.1:p.Ala699=
NM_001199041.1:c.2031C=	NP_001185970.1:p.Ala677=
NM_001199042.1:c.2103C=	NP_001185971.1:p.Ala701=
NM_022369.3:c.1986C=	NP_071764.3:p.Ala662=
XM_011521883.1:c.1986C=	XP_011520185.1:p.Ala662=
XM_011521884.1:c.1797C=	XP_011520186.1:p.Ala599=
XM_017022478.1:c.2034C=	XP_016877967.1:p.Ala678=
XM_017022479.1:c.1986C=	XP_016877968.1:p.Ala662=
XM_017022480.1:c.1797C=	XP_016877969.1:p.Ala599=
NM_022369.4:c.1986C= MANE Select	NP_071764.3:p.Ala662=
NM_001142617.2:c.1986C=	NP_001136089.1:p.Ala662=
NM_001142619.2:c.1959C=	NP_001136091.1:p.Ala653=
NM_001199042.2:c.2103C=	NP_001185971.1:p.Ala701=
NM_001142618.2:c.1986C=	NP_001136090.1:p.Ala662=
NM_001199040.2:c.2097C=	NP_001185969.1:p.Ala699=
NM_001199041.2:c.2031C=	NP_001185970.1:p.Ala677=