Canonical Allele Identifier: CA2187549622

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74179964G= , CM000677.2:g.74179964G=	GRCh38
NC_000015.9:g.74472305G= , CM000677.1:g.74472305G=	GRCh37
NC_000015.8:g.72259358G=	NCBI36
NG_009207.1:g.34067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.*116C= MANE Select	ENSP00000378537.4:n.*116C=
ENST00000323940.9:c.*116C=	ENSP00000326085.5:n.*116C=
ENST00000395105.8:c.*116C=	ENSP00000378537.4:n.*116C=
ENST00000416286.7:c.*116C=	ENSP00000400403.3:n.*116C=
ENST00000423167.6:c.*116C=	ENSP00000413012.2:n.*116C=
ENST00000449139.6:c.*116C=	ENSP00000410221.2:n.*116C=
ENST00000535552.5:c.*116C=	ENSP00000440238.1:n.*116C=
ENST00000545137.5:n.1829C=
ENST00000574439.5:n.2392C=
ENST00000616000.4:c.*116C=	ENSP00000479112.1:n.*116C=
NM_001142617.1:c.*116C=	NP_001136089.1:n.*116C=
NM_001142618.1:c.*116C=	NP_001136090.1:n.*116C=
NM_001142619.1:c.*116C=	NP_001136091.1:n.*116C=
NM_001199040.1:c.*116C=	NP_001185969.1:n.*116C=
NM_001199041.1:c.*116C=	NP_001185970.1:n.*116C=
NM_001199042.1:c.*116C=	NP_001185971.1:n.*116C=
NM_022369.3:c.*116C=	NP_071764.3:n.*116C=
XM_011521883.1:c.*116C=	XP_011520185.1:n.*116C=
XM_011521884.1:c.*116C=	XP_011520186.1:n.*116C=
XM_017022478.1:c.*116C=	XP_016877967.1:n.*116C=
XM_017022479.1:c.*116C=	XP_016877968.1:n.*116C=
XM_017022480.1:c.*116C=	XP_016877969.1:n.*116C=
NM_022369.4:c.*116C= MANE Select	NP_071764.3:n.*116C=
NM_001142617.2:c.*116C=	NP_001136089.1:n.*116C=
NM_001142619.2:c.*116C=	NP_001136091.1:n.*116C=
NM_001199042.2:c.*116C=	NP_001185971.1:n.*116C=
NM_001142618.2:c.*116C=	NP_001136090.1:n.*116C=
NM_001199040.2:c.*116C=	NP_001185969.1:n.*116C=
NM_001199041.2:c.*116C=	NP_001185970.1:n.*116C=