Canonical Allele Identifier: CA492907731
Gene: BAIAP3 HGNC NCBI

Linked Data

gnomAD v4: 16-1342784-T-C
MyVariant Identifiers: chr16:g.1392785T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1342784T>C , CM000678.2:g.1342784T>C GRCh38
NC_000016.9:g.1392785T>C , CM000678.1:g.1392785T>C GRCh37
NC_000016.8:g.1332786T>C NCBI36
NG_033974.1:g.14180T>C
NG_033974.2:g.14180T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561793.2:c.400T>C
ENST00000564213.2:c.1131T>C ENSP00000518583.1:p.His377=
ENST00000565665.6:n.1504T>C
ENST00000567203.2:n.1246T>C
ENST00000711102.1:c.1131T>C ENSP00000518580.1:p.His377=
ENST00000711103.1:c.1131T>C ENSP00000518581.1:p.His377=
ENST00000711104.1:c.1182T>C ENSP00000518582.1:p.His394=
ENST00000711105.1:c.1131T>C ENSP00000518584.1:p.His377=
ENST00000711111.1:n.1247T>C
ENST00000426824.8:c.1131T>C MANE Select ENSP00000407242.4:p.His377=
ENST00000324385.9:c.1236T>C ENSP00000324510.5:p.His412=
ENST00000397488.6:c.1182T>C ENSP00000380625.2:p.His394=
ENST00000421665.6:c.1023T>C ENSP00000409533.2:p.His341=
ENST00000426824.7:c.1131T>C ENSP00000407242.3:p.His377=
ENST00000562208.5:c.1062T>C ENSP00000458134.1:p.His354=
ENST00000568887.5:c.1047T>C ENSP00000457644.1:p.His349=
ENST00000628027.2:c.1182T>C ENSP00000487275.1:p.His394=
NM_001199096.1:c.1023T>C NP_001186025.1:p.His341=
NM_001199097.1:c.1131T>C NP_001186026.1:p.His377=
NM_001199098.1:c.1062T>C NP_001186027.1:p.His354=
NM_001199099.1:c.1047T>C NP_001186028.1:p.His349=
NM_001286464.1:c.1182T>C NP_001273393.1:p.His394=
NM_003933.4:c.1236T>C NP_003924.2:p.His412=
XM_011522728.1:c.1287T>C XP_011521030.1:p.His429=
XM_011522729.1:c.1287T>C XP_011521031.1:p.His429=
XM_011522730.1:c.1287T>C XP_011521032.1:p.His429=
XM_011522730.2:c.1287T>C XP_011521032.1:p.His429=
NM_001199097.2:c.1131T>C MANE Select NP_001186026.1:p.His377=
NM_001199098.2:c.1062T>C NP_001186027.1:p.His354=
NM_001199099.2:c.1047T>C NP_001186028.1:p.His349=
NM_001286464.2:c.1182T>C NP_001273393.2:p.His394=
NM_001199096.2:c.1023T>C NP_001186025.1:p.His341=
NM_003933.5:c.1236T>C NP_003924.2:p.His412=