Canonical Allele Identifier: CA2187554645

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190857C= , CM000677.2:g.74190857C=	GRCh38
NC_000015.9:g.74483198C= , CM000677.1:g.74483198C=	GRCh37
NC_000015.8:g.72270251C=	NCBI36
NG_009207.1:g.23174G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.910G= MANE Select	ENSP00000378537.4:p.Gly304=
ENST00000323940.9:c.910G=	ENSP00000326085.5:p.Gly304=
ENST00000395105.8:c.910G=	ENSP00000378537.4:p.Gly304=
ENST00000416286.7:c.886G=	ENSP00000400403.3:p.Gly296=
ENST00000423167.6:c.883G=	ENSP00000413012.2:p.Gly295=
ENST00000449139.6:c.910G=	ENSP00000410221.2:p.Gly304=
ENST00000535552.5:c.1021G=	ENSP00000440238.1:p.Gly341=
ENST00000545137.5:n.619G=
ENST00000563965.5:c.1027G=	ENSP00000456609.1:p.Gly343=
ENST00000569936.5:c.1040G=	ENSP00000461799.1:p.Arg347=
ENST00000574278.5:c.955G=	ENSP00000458827.1:p.Gly319=
ENST00000574439.5:n.1182G=
ENST00000616000.4:c.910G=	ENSP00000479112.1:p.Gly304=
NM_001142617.1:c.910G=	NP_001136089.1:p.Gly304=
NM_001142618.1:c.910G=	NP_001136090.1:p.Gly304=
NM_001142619.1:c.883G=	NP_001136091.1:p.Gly295=
NM_001199040.1:c.1021G=	NP_001185969.1:p.Gly341=
NM_001199041.1:c.955G=	NP_001185970.1:p.Gly319=
NM_001199042.1:c.1027G=	NP_001185971.1:p.Gly343=
NM_022369.3:c.910G=	NP_071764.3:p.Gly304=
XM_011521883.1:c.910G=	XP_011520185.1:p.Gly304=
XM_011521884.1:c.721G=	XP_011520186.1:p.Gly241=
XM_011521885.1:c.1027G=	XP_011520187.1:p.Gly343=
XR_931877.1:n.1033G=
XM_011521885.2:c.1027G=	XP_011520187.1:p.Gly343=
XM_017022478.1:c.958G=	XP_016877967.1:p.Gly320=
XM_017022479.1:c.910G=	XP_016877968.1:p.Gly304=
XM_017022480.1:c.721G=	XP_016877969.1:p.Gly241=
XR_931877.2:n.1033G=
NM_022369.4:c.910G= MANE Select	NP_071764.3:p.Gly304=
NM_001142617.2:c.910G=	NP_001136089.1:p.Gly304=
NM_001142619.2:c.883G=	NP_001136091.1:p.Gly295=
NM_001199042.2:c.1027G=	NP_001185971.1:p.Gly343=
NM_001142618.2:c.910G=	NP_001136090.1:p.Gly304=
NM_001199040.2:c.1021G=	NP_001185969.1:p.Gly341=
NM_001199041.2:c.955G=	NP_001185970.1:p.Gly319=