Canonical Allele Identifier: CA394164495

Gene: BAIAP3

Linked Data

• MyVariant Identifiers: chr16:g.1392768C>G (hg19) ; chr16:g.1342767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342767C>G , CM000678.2:g.1342767C>G	GRCh38
NC_000016.9:g.1392768C>G , CM000678.1:g.1392768C>G	GRCh37
NC_000016.8:g.1332769C>G	NCBI36
NG_033974.1:g.14163C>G
NG_033974.2:g.14163C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.383C>G
ENST00000564213.2:c.1114C>G	ENSP00000518583.1:p.Leu372Val
ENST00000565665.6:n.1487C>G
ENST00000567203.2:n.1229C>G
ENST00000711102.1:c.1114C>G	ENSP00000518580.1:p.Leu372Val
ENST00000711103.1:c.1114C>G	ENSP00000518581.1:p.Leu372Val
ENST00000711104.1:c.1165C>G	ENSP00000518582.1:p.Leu389Val
ENST00000711105.1:c.1114C>G	ENSP00000518584.1:p.Leu372Val
ENST00000711111.1:n.1230C>G
ENST00000426824.8:c.1114C>G MANE Select	ENSP00000407242.4:p.Leu372Val
ENST00000324385.9:c.1219C>G	ENSP00000324510.5:p.Leu407Val
ENST00000397488.6:c.1165C>G	ENSP00000380625.2:p.Leu389Val
ENST00000421665.6:c.1006C>G	ENSP00000409533.2:p.Leu336Val
ENST00000426824.7:c.1114C>G	ENSP00000407242.3:p.Leu372Val
ENST00000562208.5:c.1045C>G	ENSP00000458134.1:p.Leu349Val
ENST00000568887.5:c.1030C>G	ENSP00000457644.1:p.Leu344Val
ENST00000628027.2:c.1165C>G	ENSP00000487275.1:p.Leu389Val
NM_001199096.1:c.1006C>G	NP_001186025.1:p.Leu336Val
NM_001199097.1:c.1114C>G	NP_001186026.1:p.Leu372Val
NM_001199098.1:c.1045C>G	NP_001186027.1:p.Leu349Val
NM_001199099.1:c.1030C>G	NP_001186028.1:p.Leu344Val
NM_001286464.1:c.1165C>G	NP_001273393.1:p.Leu389Val
NM_003933.4:c.1219C>G	NP_003924.2:p.Leu407Val
XM_011522728.1:c.1270C>G	XP_011521030.1:p.Leu424Val
XM_011522729.1:c.1270C>G	XP_011521031.1:p.Leu424Val
XM_011522730.1:c.1270C>G	XP_011521032.1:p.Leu424Val
XM_011522730.2:c.1270C>G	XP_011521032.1:p.Leu424Val
NM_001199097.2:c.1114C>G MANE Select	NP_001186026.1:p.Leu372Val
NM_001199098.2:c.1045C>G	NP_001186027.1:p.Leu349Val
NM_001199099.2:c.1030C>G	NP_001186028.1:p.Leu344Val
NM_001286464.2:c.1165C>G	NP_001273393.2:p.Leu389Val
NM_001199096.2:c.1006C>G	NP_001186025.1:p.Leu336Val
NM_003933.5:c.1219C>G	NP_003924.2:p.Leu407Val