Canonical Allele Identifier: CA394169753

Gene: BAIAP3

Linked Data

• gnomAD v4: 16-1347818-A-G
• MyVariant Identifiers: chr16:g.1397819A>G (hg19) ; chr16:g.1347818A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1347818A>G , CM000678.2:g.1347818A>G	GRCh38
NC_000016.9:g.1397819A>G , CM000678.1:g.1397819A>G	GRCh37
NC_000016.8:g.1337820A>G	NCBI36
NG_016985.1:g.920A>G
NG_033974.1:g.19214A>G
NG_033974.2:g.19214A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561793.2:c.2204A>G
ENST00000564213.2:c.*216A>G	ENSP00000518583.1:n.*216A>G
ENST00000565665.6:n.3286A>G
ENST00000567203.2:n.3641A>G
ENST00000568198.2:n.1803A>G
ENST00000711102.1:c.3022A>G	ENSP00000518580.1:p.Asn1008Asp
ENST00000711103.1:c.*1205A>G	ENSP00000518581.1:n.*1205A>G
ENST00000711104.1:c.*216A>G	ENSP00000518582.1:n.*216A>G
ENST00000711105.1:c.2959A>G	ENSP00000518584.1:p.Asn987Asp
ENST00000711106.1:c.1681A>G	ENSP00000518585.1:p.Asn561Asp
ENST00000711107.1:c.1618A>G	ENSP00000518586.1:p.Asn540Asp
ENST00000711108.1:c.1681A>G	ENSP00000518587.1:p.Asn561Asp
ENST00000711109.1:c.*1063A>G	ENSP00000518588.1:n.*1063A>G
ENST00000711110.1:c.340A>G	ENSP00000518589.1:p.Asn114Asp
ENST00000711111.1:n.3364A>G
ENST00000426824.8:c.3022A>G MANE Select	ENSP00000407242.4:p.Asn1008Asp
ENST00000324385.9:c.3127A>G	ENSP00000324510.5:p.Asn1043Asp
ENST00000397488.6:c.3073A>G	ENSP00000380625.2:p.Asn1025Asp
ENST00000421665.6:c.2914A>G	ENSP00000409533.2:p.Asn972Asp
ENST00000426824.7:c.3022A>G	ENSP00000407242.3:p.Asn1008Asp
ENST00000562208.5:c.2953A>G	ENSP00000458134.1:p.Asn985Asp
ENST00000566162.1:c.627-1548A>G
ENST00000566389.1:n.508A>G
ENST00000568887.5:c.2938A>G	ENSP00000457644.1:p.Asn980Asp
ENST00000628027.2:c.3073A>G	ENSP00000487275.1:p.Asn1025Asp
NM_001199096.1:c.2914A>G	NP_001186025.1:p.Asn972Asp
NM_001199097.1:c.3022A>G	NP_001186026.1:p.Asn1008Asp
NM_001199098.1:c.2953A>G	NP_001186027.1:p.Asn985Asp
NM_001199099.1:c.2938A>G	NP_001186028.1:p.Asn980Asp
NM_001286464.1:c.3073A>G	NP_001273393.1:p.Asn1025Asp
NM_003933.4:c.3127A>G	NP_003924.2:p.Asn1043Asp
XM_011522728.1:c.3178A>G	XP_011521030.1:p.Asn1060Asp
XM_011522729.1:c.3178A>G	XP_011521031.1:p.Asn1060Asp
XM_011522730.1:c.3178A>G	XP_011521032.1:p.Asn1060Asp
XM_011522730.2:c.3178A>G	XP_011521032.1:p.Asn1060Asp
NM_001199097.2:c.3022A>G MANE Select	NP_001186026.1:p.Asn1008Asp
NM_001199098.2:c.2953A>G	NP_001186027.1:p.Asn985Asp
NM_001199099.2:c.2938A>G	NP_001186028.1:p.Asn980Asp
NM_001286464.2:c.3073A>G	NP_001273393.2:p.Asn1025Asp
NM_001199096.2:c.2914A>G	NP_001186025.1:p.Asn972Asp
NM_003933.5:c.3127A>G	NP_003924.2:p.Asn1043Asp