Canonical Allele Identifier: CA7805845

Gene: BAIAP3

Linked Data

• dbSNP Id: rs2235632
• ExAC: 16:1393020 G / A
• gnomAD: 16:1393020 G / A
• MyVariant Identifiers: chr16:g.1393020G>A (hg19) ; chr16:g.1343019G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1343019G>A , CM000678.2:g.1343019G>A	GRCh38
NC_000016.9:g.1393020G>A , CM000678.1:g.1393020G>A	GRCh37
NC_000016.8:g.1333021G>A	NCBI36
NG_033974.1:g.14415G>A
NG_033974.2:g.14415G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426824.8:c.1265+3G>A MANE Select	ENSP00000407242.4:p.=
ENST00000324385.9:c.1370+3G>A	ENSP00000324510.5:p.=
ENST00000397488.6:c.1316+3G>A	ENSP00000380625.2:p.=
ENST00000421665.6:c.1157+3G>A	ENSP00000409533.2:p.=
ENST00000426824.7:c.1265+3G>A	ENSP00000407242.3:p.=
ENST00000562208.5:c.1196+3G>A	ENSP00000458134.1:p.=
ENST00000568887.5:c.1181+3G>A	ENSP00000457644.1:p.=
ENST00000628027.2:c.1316+3G>A	ENSP00000487275.1:p.=
NM_001199096.1:c.1157+3G>A	NP_001186025.1:p.=
NM_001199097.1:c.1265+3G>A	NP_001186026.1:p.=
NM_001199098.1:c.1196+3G>A	NP_001186027.1:p.=
NM_001199099.1:c.1181+3G>A	NP_001186028.1:p.=
NM_001286464.1:c.1316+3G>A	NP_001273393.1:p.=
NM_003933.4:c.1370+3G>A	NP_003924.2:p.=
XM_011522728.1:c.1421+3G>A	XP_011521030.1:p.=
XM_011522729.1:c.1421+3G>A	XP_011521031.1:p.=
XM_011522730.1:c.1421+3G>A	XP_011521032.1:p.=
XM_011522730.2:c.1421+3G>A	XP_011521032.1:p.=
NM_001199097.2:c.1265+3G>A MANE Select	NP_001186026.1:p.=
NM_001199098.2:c.1196+3G>A	NP_001186027.1:p.=
NM_001199099.2:c.1181+3G>A	NP_001186028.1:p.=
NM_001286464.2:c.1316+3G>A	NP_001273393.2:p.=
NM_001199096.2:c.1157+3G>A	NP_001186025.1:p.=
NM_003933.5:c.1370+3G>A	NP_003924.2:p.=