Canonical Allele Identifier: CA2201601477

Gene: BAIAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342764C= , CM000678.2:g.1342764C=	GRCh38
NC_000016.9:g.1392765C= , CM000678.1:g.1392765C=	GRCh37
NC_000016.8:g.1332766C=	NCBI36
NG_033974.1:g.14160C=
NG_033974.2:g.14160C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.380C=
ENST00000564213.2:c.1111C=	ENSP00000518583.1:p.His371=
ENST00000565665.6:n.1484C=
ENST00000567203.2:n.1226C=
ENST00000711102.1:c.1111C=	ENSP00000518580.1:p.His371=
ENST00000711103.1:c.1111C=	ENSP00000518581.1:p.His371=
ENST00000711104.1:c.1162C=	ENSP00000518582.1:p.His388=
ENST00000711105.1:c.1111C=	ENSP00000518584.1:p.His371=
ENST00000711111.1:n.1227C=
ENST00000426824.8:c.1111C= MANE Select	ENSP00000407242.4:p.His371=
ENST00000324385.9:c.1216C=	ENSP00000324510.5:p.His406=
ENST00000397488.6:c.1162C=	ENSP00000380625.2:p.His388=
ENST00000421665.6:c.1003C=	ENSP00000409533.2:p.His335=
ENST00000426824.7:c.1111C=	ENSP00000407242.3:p.His371=
ENST00000562208.5:c.1042C=	ENSP00000458134.1:p.His348=
ENST00000568887.5:c.1027C=	ENSP00000457644.1:p.His343=
ENST00000628027.2:c.1162C=	ENSP00000487275.1:p.His388=
NM_001199096.1:c.1003C=	NP_001186025.1:p.His335=
NM_001199097.1:c.1111C=	NP_001186026.1:p.His371=
NM_001199098.1:c.1042C=	NP_001186027.1:p.His348=
NM_001199099.1:c.1027C=	NP_001186028.1:p.His343=
NM_001286464.1:c.1162C=	NP_001273393.1:p.His388=
NM_003933.4:c.1216C=	NP_003924.2:p.His406=
XM_011522728.1:c.1267C=	XP_011521030.1:p.His423=
XM_011522729.1:c.1267C=	XP_011521031.1:p.His423=
XM_011522730.1:c.1267C=	XP_011521032.1:p.His423=
XM_011522730.2:c.1267C=	XP_011521032.1:p.His423=
NM_001199097.2:c.1111C= MANE Select	NP_001186026.1:p.His371=
NM_001199098.2:c.1042C=	NP_001186027.1:p.His348=
NM_001199099.2:c.1027C=	NP_001186028.1:p.His343=
NM_001286464.2:c.1162C=	NP_001273393.2:p.His388=
NM_001199096.2:c.1003C=	NP_001186025.1:p.His335=
NM_003933.5:c.1216C=	NP_003924.2:p.His406=