Canonical Allele Identifier: CA129967729

Gene: SPARC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151676131C>G , CM000667.2:g.151676131C>G	GRCh38
NC_000005.9:g.151055692C>G , CM000667.1:g.151055692C>G	GRCh37
NC_000005.8:g.151035885C>G	NCBI36
NG_042174.1:g.15924G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003118.4:c.57+1G>C MANE Select	NP_003109.1:n.57+1G>C
ENST00000231061.9:c.57+1G>C MANE Select	ENSP00000231061.4:n.57+1G>C
NM_001309443.1:c.57+1G>C	NP_001296372.1:n.57+1G>C
NM_001309443.2:c.57+1G>C	NP_001296372.1:n.57+1G>C
NM_001309444.1:c.57+1G>C	NP_001296373.1:n.57+1G>C
NM_001309444.2:c.57+1G>C	NP_001296373.1:n.57+1G>C
NM_003118.3:c.57+1G>C	NP_003109.1:n.57+1G>C
ENST00000231061.8:c.57+1G>C	ENSP00000231061.4:n.57+1G>C
ENST00000521327.1:n.181+1G>C
ENST00000521569.1:c.-153-2915G>C	ENSP00000428119.1:n.-153-2915G>C
ENST00000522348.1:c.57+1G>C	ENSP00000429152.1:n.57+1G>C
ENST00000538026.5:c.-65-4437G>C	ENSP00000440127.1:n.-65-4437G>C
ENST00000539687.5:c.57+1G>C	ENSP00000444998.1:n.57+1G>C
ENST00000539687.6:c.57+1G>C	ENSP00000444998.2:n.57+1G>C