Canonical Allele Identifier: CA3522824

Gene: SPARC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151674607C>T , CM000667.2:g.151674607C>T	GRCh38
NC_000005.9:g.151054168C>T , CM000667.1:g.151054168C>T	GRCh37
NC_000005.8:g.151034361C>T	NCBI36
NG_042174.1:g.17448G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003118.4:c.120+5G>A MANE Select	NP_003109.1:n.120+5G>A
ENST00000231061.9:c.120+5G>A MANE Select	ENSP00000231061.4:n.120+5G>A
NM_001309443.1:c.117+5G>A	NP_001296372.1:n.117+5G>A
NM_001309443.2:c.117+5G>A	NP_001296372.1:n.117+5G>A
NM_001309444.1:c.120+5G>A	NP_001296373.1:n.120+5G>A
NM_001309444.2:c.120+5G>A	NP_001296373.1:n.120+5G>A
NM_003118.3:c.120+5G>A	NP_003109.1:n.120+5G>A
ENST00000231061.8:c.120+5G>A	ENSP00000231061.4:n.120+5G>A
ENST00000521327.1:n.244+5G>A
ENST00000521569.1:c.-153-1391G>A	ENSP00000428119.1:n.-153-1391G>A
ENST00000522348.1:c.120+5G>A	ENSP00000429152.1:n.120+5G>A
ENST00000538026.5:c.-65-2913G>A	ENSP00000440127.1:n.-65-2913G>A
ENST00000539687.5:c.120+5G>A	ENSP00000444998.1:n.120+5G>A
ENST00000539687.6:c.120+5G>A	ENSP00000444998.2:n.120+5G>A