Canonical Allele Identifier: CA361832433
Community Standard Title: NM_003118.4(SPARC):c.497G>C (p.Arg166Pro)
Gene: SPARC HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_003118.4:c.497G>C MANE Select NP_003109.1:p.Arg166Pro
ENST00000231061.9:c.497G>C MANE Select ENSP00000231061.4:p.Arg166Pro
NM_001309443.1:c.494G>C NP_001296372.1:p.Arg165Pro
NM_001309443.2:c.494G>C NP_001296372.1:p.Arg165Pro
NM_001309444.1:c.497G>C NP_001296373.1:p.Arg166Pro
NM_001309444.2:c.497G>C NP_001296373.1:p.Arg166Pro
NM_003118.3:c.497G>C NP_003109.1:p.Arg166Pro
ENST00000231061.8:c.497G>C ENSP00000231061.4:p.Arg166Pro
ENST00000520687.1:n.100G>C
ENST00000521569.1:c.224G>C ENSP00000428119.1:p.Arg75Pro
ENST00000524277.1:n.424G>C
ENST00000537849.1:n.30G>C
ENST00000538026.5:c.224G>C ENSP00000440127.1:p.Arg75Pro