Canonical Allele Identifier: CA1591490319

Gene: SPARC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151667555C= , CM000667.2:g.151667555C=	GRCh38
NC_000005.9:g.151047116C= , CM000667.1:g.151047116C=	GRCh37
NC_000005.8:g.151027309C=	NCBI36
NG_042174.1:g.24500G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003118.4:c.497G= MANE Select	NP_003109.1:p.Arg166=
ENST00000231061.9:c.497G= MANE Select	ENSP00000231061.4:p.Arg166=
NM_001309443.1:c.494G=	NP_001296372.1:p.Arg165=
NM_001309443.2:c.494G=	NP_001296372.1:p.Arg165=
NM_001309444.1:c.497G=	NP_001296373.1:p.Arg166=
NM_001309444.2:c.497G=	NP_001296373.1:p.Arg166=
NM_003118.3:c.497G=	NP_003109.1:p.Arg166=
ENST00000231061.8:c.497G=	ENSP00000231061.4:p.Arg166=
ENST00000520687.1:n.100G=
ENST00000521569.1:c.224G=	ENSP00000428119.1:p.Arg75=
ENST00000524277.1:n.424G=
ENST00000537849.1:n.30G=
ENST00000538026.5:c.224G=	ENSP00000440127.1:p.Arg75=