Canonical Allele Identifier: CA492907752

Gene: BAIAP3

Linked Data

• MyVariant Identifiers: chr16:g.1392809A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342808A>T , CM000678.2:g.1342808A>T	GRCh38
NC_000016.9:g.1392809A>T , CM000678.1:g.1392809A>T	GRCh37
NC_000016.8:g.1332810A>T	NCBI36
NG_033974.1:g.14204A>T
NG_033974.2:g.14204A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.424A>T
ENST00000564213.2:c.1155A>T	ENSP00000518583.1:p.Ala385=
ENST00000565665.6:n.1528A>T
ENST00000567203.2:n.1270A>T
ENST00000711102.1:c.1155A>T	ENSP00000518580.1:p.Ala385=
ENST00000711103.1:c.1155A>T	ENSP00000518581.1:p.Ala385=
ENST00000711104.1:c.1206A>T	ENSP00000518582.1:p.Ala402=
ENST00000711105.1:c.1155A>T	ENSP00000518584.1:p.Ala385=
ENST00000711111.1:n.1271A>T
ENST00000426824.8:c.1155A>T MANE Select	ENSP00000407242.4:p.Ala385=
ENST00000324385.9:c.1260A>T	ENSP00000324510.5:p.Ala420=
ENST00000397488.6:c.1206A>T	ENSP00000380625.2:p.Ala402=
ENST00000421665.6:c.1047A>T	ENSP00000409533.2:p.Ala349=
ENST00000426824.7:c.1155A>T	ENSP00000407242.3:p.Ala385=
ENST00000562208.5:c.1086A>T	ENSP00000458134.1:p.Ala362=
ENST00000568887.5:c.1071A>T	ENSP00000457644.1:p.Ala357=
ENST00000628027.2:c.1206A>T	ENSP00000487275.1:p.Ala402=
NM_001199096.1:c.1047A>T	NP_001186025.1:p.Ala349=
NM_001199097.1:c.1155A>T	NP_001186026.1:p.Ala385=
NM_001199098.1:c.1086A>T	NP_001186027.1:p.Ala362=
NM_001199099.1:c.1071A>T	NP_001186028.1:p.Ala357=
NM_001286464.1:c.1206A>T	NP_001273393.1:p.Ala402=
NM_003933.4:c.1260A>T	NP_003924.2:p.Ala420=
XM_011522728.1:c.1311A>T	XP_011521030.1:p.Ala437=
XM_011522729.1:c.1311A>T	XP_011521031.1:p.Ala437=
XM_011522730.1:c.1311A>T	XP_011521032.1:p.Ala437=
XM_011522730.2:c.1311A>T	XP_011521032.1:p.Ala437=
NM_001199097.2:c.1155A>T MANE Select	NP_001186026.1:p.Ala385=
NM_001199098.2:c.1086A>T	NP_001186027.1:p.Ala362=
NM_001199099.2:c.1071A>T	NP_001186028.1:p.Ala357=
NM_001286464.2:c.1206A>T	NP_001273393.2:p.Ala402=
NM_001199096.2:c.1047A>T	NP_001186025.1:p.Ala349=
NM_003933.5:c.1260A>T	NP_003924.2:p.Ala420=