Canonical Allele Identifier: CA2838210109

Gene: DAZAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1432787C>G , CM000681.2:g.1432787C>G	GRCh38
NC_000019.9:g.1432786C>G , CM000681.1:g.1432786C>G	GRCh37
NC_000019.8:g.1383786C>G	NCBI36
NG_029884.1:g.30203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233078.9:c.1048+97C>G MANE Select	ENSP00000233078.4:n.1048+97C>G
ENST00000233078.8:c.1048+97C>G	ENSP00000233078.3:n.1048+97C>G
ENST00000336761.10:c.1048+97C>G	ENSP00000337132.5:n.1048+97C>G
ENST00000585485.2:n.2995+97C>G
ENST00000587079.5:c.1045+97C>G	ENSP00000465433.2:n.1045+97C>G
ENST00000589484.5:n.2466+97C>G
ENST00000589874.2:n.745C>G
ENST00000592522.5:c.1048+97C>G	ENSP00000467680.2:n.1048+97C>G
NM_018959.3:c.1048+97C>G	NP_061832.2:n.1048+97C>G
NM_170711.2:c.1048+97C>G	NP_733829.1:n.1048+97C>G
XM_005259531.2:c.1045+97C>G	XP_005259588.1:n.1045+97C>G
XM_005259534.2:c.529+97C>G	XP_005259591.1:n.529+97C>G
XM_005259535.2:c.529+97C>G	XP_005259592.1:n.529+97C>G
XM_005259536.2:c.529+97C>G	XP_005259593.1:n.529+97C>G
XM_011527904.1:c.1477+97C>G	XP_011526206.1:n.1477+97C>G
XM_011527905.1:c.1477+97C>G	XP_011526207.1:n.1477+97C>G
XM_011527906.1:c.1474+97C>G	XP_011526208.1:n.1474+97C>G
XM_011527907.1:c.1474+97C>G	XP_011526209.1:n.1474+97C>G
XM_011527908.1:c.1477+97C>G	XP_011526210.1:n.1477+97C>G
XM_011527909.1:c.1477+97C>G	XP_011526211.1:n.1477+97C>G
XM_011527910.1:c.925+97C>G	XP_011526212.1:n.925+97C>G
NM_001352033.1:c.1045+97C>G	NP_001338962.1:n.1045+97C>G
NM_001352034.1:c.1048+97C>G	NP_001338963.1:n.1048+97C>G
NM_001352035.1:c.529+97C>G	NP_001338964.1:n.529+97C>G
XM_005259535.3:c.529+97C>G	XP_005259592.1:n.529+97C>G
XM_005259536.4:c.529+97C>G	XP_005259593.1:n.529+97C>G
XM_011527904.2:c.1477+97C>G	XP_011526206.1:n.1477+97C>G
XM_011527905.2:c.1477+97C>G	XP_011526207.1:n.1477+97C>G
XM_011527906.2:c.1474+97C>G	XP_011526208.1:n.1474+97C>G
XM_011527907.2:c.1474+97C>G	XP_011526209.1:n.1474+97C>G
XM_011527908.2:c.1477+97C>G	XP_011526210.1:n.1477+97C>G
XM_011527909.3:c.1477+97C>G	XP_011526211.1:n.1477+97C>G
XM_011527910.2:c.925+97C>G	XP_011526212.1:n.925+97C>G
NM_001352033.2:c.1045+97C>G	NP_001338962.1:n.1045+97C>G
NM_001352034.2:c.1048+97C>G	NP_001338963.1:n.1048+97C>G
NM_001352035.2:c.529+97C>G	NP_001338964.1:n.529+97C>G
NM_018959.4:c.1048+97C>G MANE Select	NP_061832.2:n.1048+97C>G
NM_170711.3:c.1048+97C>G	NP_733829.1:n.1048+97C>G