Canonical Allele Identifier: CA718220494

Gene: BAIAP3

Linked Data

• dbSNP Id: rs1203027454
• MyVariant Identifiers: chr16:g.1393037_1393038insGTGGGCGGGGAAT (hg19) ; chr16:g.1343036_1343037insGTGGGCGGGGAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1343046_1343058dup , CM000678.2:g.1343046_1343058dup	GRCh38
NC_000016.9:g.1393047_1393059dup , CM000678.1:g.1393047_1393059dup	GRCh37
NC_000016.8:g.1333048_1333060dup	NCBI36
NG_033974.1:g.14442_14454dup
NG_033974.2:g.14442_14454dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.534+30_534+42dup
ENST00000564213.2:c.1265+30_1265+42dup	ENSP00000518583.1:n.1265+30_1265+42dup
ENST00000565665.6:n.1638+30_1638+42dup
ENST00000567203.2:n.1380+30_1380+42dup
ENST00000711102.1:c.1265+30_1265+42dup	ENSP00000518580.1:n.1265+30_1265+42dup
ENST00000711103.1:c.1265+30_1265+42dup	ENSP00000518581.1:n.1265+30_1265+42dup
ENST00000711104.1:c.1316+30_1316+42dup	ENSP00000518582.1:n.1316+30_1316+42dup
ENST00000711105.1:c.1265+30_1265+42dup	ENSP00000518584.1:n.1265+30_1265+42dup
ENST00000711111.1:n.1381+30_1381+42dup
ENST00000426824.8:c.1265+30_1265+42dup MANE Select	ENSP00000407242.4:n.1265+30_1265+42dup
ENST00000324385.9:c.1370+30_1370+42dup	ENSP00000324510.5:n.1370+30_1370+42dup
ENST00000397488.6:c.1316+30_1316+42dup	ENSP00000380625.2:n.1316+30_1316+42dup
ENST00000421665.6:c.1157+30_1157+42dup	ENSP00000409533.2:n.1157+30_1157+42dup
ENST00000426824.7:c.1265+30_1265+42dup	ENSP00000407242.3:n.1265+30_1265+42dup
ENST00000562208.5:c.1196+30_1196+42dup	ENSP00000458134.1:n.1196+30_1196+42dup
ENST00000568887.5:c.1181+30_1181+42dup	ENSP00000457644.1:n.1181+30_1181+42dup
ENST00000628027.2:c.1316+30_1316+42dup	ENSP00000487275.1:n.1316+30_1316+42dup
NM_001199096.1:c.1157+30_1157+42dup	NP_001186025.1:n.1157+30_1157+42dup
NM_001199097.1:c.1265+30_1265+42dup	NP_001186026.1:n.1265+30_1265+42dup
NM_001199098.1:c.1196+30_1196+42dup	NP_001186027.1:n.1196+30_1196+42dup
NM_001199099.1:c.1181+30_1181+42dup	NP_001186028.1:n.1181+30_1181+42dup
NM_001286464.1:c.1316+30_1316+42dup	NP_001273393.1:n.1316+30_1316+42dup
NM_003933.4:c.1370+30_1370+42dup	NP_003924.2:n.1370+30_1370+42dup
XM_011522728.1:c.1421+30_1421+42dup	XP_011521030.1:n.1421+30_1421+42dup
XM_011522729.1:c.1421+30_1421+42dup	XP_011521031.1:n.1421+30_1421+42dup
XM_011522730.1:c.1421+30_1421+42dup	XP_011521032.1:n.1421+30_1421+42dup
XM_011522730.2:c.1421+30_1421+42dup	XP_011521032.1:n.1421+30_1421+42dup
NM_001199097.2:c.1265+30_1265+42dup MANE Select	NP_001186026.1:n.1265+30_1265+42dup
NM_001199098.2:c.1196+30_1196+42dup	NP_001186027.1:n.1196+30_1196+42dup
NM_001199099.2:c.1181+30_1181+42dup	NP_001186028.1:n.1181+30_1181+42dup
NM_001286464.2:c.1316+30_1316+42dup	NP_001273393.2:n.1316+30_1316+42dup
NM_001199096.2:c.1157+30_1157+42dup	NP_001186025.1:n.1157+30_1157+42dup
NM_003933.5:c.1370+30_1370+42dup	NP_003924.2:n.1370+30_1370+42dup