Canonical Allele Identifier: CA129959069
Community Standard Title: NM_003118.4(SPARC):c.884-140G>A
Gene: SPARC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151663739C>T , CM000667.2:g.151663739C>T GRCh38
NC_000005.9:g.151043300C>T , CM000667.1:g.151043300C>T GRCh37
NC_000005.8:g.151023493C>T NCBI36
NG_042174.1:g.28316G>A

Transcript Alleles

HGVS Amino-acid Change
NM_003118.4:c.884-140G>A MANE Select NP_003109.1:n.884-140G>A
ENST00000231061.9:c.884-140G>A MANE Select ENSP00000231061.4:n.884-140G>A
NM_001309443.1:c.881-140G>A NP_001296372.1:n.881-140G>A
NM_001309443.2:c.881-140G>A NP_001296372.1:n.881-140G>A
NM_001309444.1:c.884-142G>A NP_001296373.1:n.884-142G>A
NM_001309444.2:c.884-142G>A NP_001296373.1:n.884-142G>A
NM_003118.3:c.884-140G>A NP_003109.1:n.884-140G>A
ENST00000231061.8:c.884-140G>A ENSP00000231061.4:n.884-140G>A
ENST00000520687.1:n.487-140G>A