Canonical Allele Identifier: CA394164436

Gene: BAIAP3

Linked Data

• MyVariant Identifiers: chr16:g.1392754G>C (hg19) ; chr16:g.1342753G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342753G>C , CM000678.2:g.1342753G>C	GRCh38
NC_000016.9:g.1392754G>C , CM000678.1:g.1392754G>C	GRCh37
NC_000016.8:g.1332755G>C	NCBI36
NG_033974.1:g.14149G>C
NG_033974.2:g.14149G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.369G>C
ENST00000564213.2:c.1100G>C	ENSP00000518583.1:p.Gly367Ala
ENST00000565665.6:n.1473G>C
ENST00000567203.2:n.1215G>C
ENST00000711102.1:c.1100G>C	ENSP00000518580.1:p.Gly367Ala
ENST00000711103.1:c.1100G>C	ENSP00000518581.1:p.Gly367Ala
ENST00000711104.1:c.1151G>C	ENSP00000518582.1:p.Gly384Ala
ENST00000711105.1:c.1100G>C	ENSP00000518584.1:p.Gly367Ala
ENST00000711111.1:n.1216G>C
ENST00000426824.8:c.1100G>C MANE Select	ENSP00000407242.4:p.Gly367Ala
ENST00000324385.9:c.1205G>C	ENSP00000324510.5:p.Gly402Ala
ENST00000397488.6:c.1151G>C	ENSP00000380625.2:p.Gly384Ala
ENST00000421665.6:c.992G>C	ENSP00000409533.2:p.Gly331Ala
ENST00000426824.7:c.1100G>C	ENSP00000407242.3:p.Gly367Ala
ENST00000562208.5:c.1031G>C	ENSP00000458134.1:p.Gly344Ala
ENST00000568887.5:c.1016G>C	ENSP00000457644.1:p.Gly339Ala
ENST00000628027.2:c.1151G>C	ENSP00000487275.1:p.Gly384Ala
NM_001199096.1:c.992G>C	NP_001186025.1:p.Gly331Ala
NM_001199097.1:c.1100G>C	NP_001186026.1:p.Gly367Ala
NM_001199098.1:c.1031G>C	NP_001186027.1:p.Gly344Ala
NM_001199099.1:c.1016G>C	NP_001186028.1:p.Gly339Ala
NM_001286464.1:c.1151G>C	NP_001273393.1:p.Gly384Ala
NM_003933.4:c.1205G>C	NP_003924.2:p.Gly402Ala
XM_011522728.1:c.1256G>C	XP_011521030.1:p.Gly419Ala
XM_011522729.1:c.1256G>C	XP_011521031.1:p.Gly419Ala
XM_011522730.1:c.1256G>C	XP_011521032.1:p.Gly419Ala
XM_011522730.2:c.1256G>C	XP_011521032.1:p.Gly419Ala
NM_001199097.2:c.1100G>C MANE Select	NP_001186026.1:p.Gly367Ala
NM_001199098.2:c.1031G>C	NP_001186027.1:p.Gly344Ala
NM_001199099.2:c.1016G>C	NP_001186028.1:p.Gly339Ala
NM_001286464.2:c.1151G>C	NP_001273393.2:p.Gly384Ala
NM_001199096.2:c.992G>C	NP_001186025.1:p.Gly331Ala
NM_003933.5:c.1205G>C	NP_003924.2:p.Gly402Ala