Canonical Allele Identifier: CA394169770

Gene: BAIAP3

Linked Data

• gnomAD v4: 16-1347821-G-T
• MyVariant Identifiers: chr16:g.1397822G>T (hg19) ; chr16:g.1347821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1347821G>T , CM000678.2:g.1347821G>T	GRCh38
NC_000016.9:g.1397822G>T , CM000678.1:g.1397822G>T	GRCh37
NC_000016.8:g.1337823G>T	NCBI36
NG_016985.1:g.923G>T
NG_033974.1:g.19217G>T
NG_033974.2:g.19217G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000561793.2:c.2207G>T
ENST00000564213.2:c.*219G>T	ENSP00000518583.1:n.*219G>T
ENST00000565665.6:n.3289G>T
ENST00000567203.2:n.3644G>T
ENST00000568198.2:n.1806G>T
ENST00000711102.1:c.3025G>T	ENSP00000518580.1:p.Gly1009Cys
ENST00000711103.1:c.*1208G>T	ENSP00000518581.1:n.*1208G>T
ENST00000711104.1:c.*219G>T	ENSP00000518582.1:n.*219G>T
ENST00000711105.1:c.2962G>T	ENSP00000518584.1:p.Gly988Cys
ENST00000711106.1:c.1684G>T	ENSP00000518585.1:p.Gly562Cys
ENST00000711107.1:c.1621G>T	ENSP00000518586.1:p.Gly541Cys
ENST00000711108.1:c.1684G>T	ENSP00000518587.1:p.Gly562Cys
ENST00000711109.1:c.*1066G>T	ENSP00000518588.1:n.*1066G>T
ENST00000711110.1:c.343G>T	ENSP00000518589.1:p.Gly115Cys
ENST00000711111.1:n.3367G>T
ENST00000426824.8:c.3025G>T MANE Select	ENSP00000407242.4:p.Gly1009Cys
ENST00000324385.9:c.3130G>T	ENSP00000324510.5:p.Gly1044Cys
ENST00000397488.6:c.3076G>T	ENSP00000380625.2:p.Gly1026Cys
ENST00000421665.6:c.2917G>T	ENSP00000409533.2:p.Gly973Cys
ENST00000426824.7:c.3025G>T	ENSP00000407242.3:p.Gly1009Cys
ENST00000562208.5:c.2956G>T	ENSP00000458134.1:p.Gly986Cys
ENST00000566162.1:c.627-1545G>T
ENST00000566389.1:n.511G>T
ENST00000568887.5:c.2941G>T	ENSP00000457644.1:p.Gly981Cys
ENST00000628027.2:c.3076G>T	ENSP00000487275.1:p.Gly1026Cys
NM_001199096.1:c.2917G>T	NP_001186025.1:p.Gly973Cys
NM_001199097.1:c.3025G>T	NP_001186026.1:p.Gly1009Cys
NM_001199098.1:c.2956G>T	NP_001186027.1:p.Gly986Cys
NM_001199099.1:c.2941G>T	NP_001186028.1:p.Gly981Cys
NM_001286464.1:c.3076G>T	NP_001273393.1:p.Gly1026Cys
NM_003933.4:c.3130G>T	NP_003924.2:p.Gly1044Cys
XM_011522728.1:c.3181G>T	XP_011521030.1:p.Gly1061Cys
XM_011522729.1:c.3181G>T	XP_011521031.1:p.Gly1061Cys
XM_011522730.1:c.3181G>T	XP_011521032.1:p.Gly1061Cys
XM_011522730.2:c.3181G>T	XP_011521032.1:p.Gly1061Cys
NM_001199097.2:c.3025G>T MANE Select	NP_001186026.1:p.Gly1009Cys
NM_001199098.2:c.2956G>T	NP_001186027.1:p.Gly986Cys
NM_001199099.2:c.2941G>T	NP_001186028.1:p.Gly981Cys
NM_001286464.2:c.3076G>T	NP_001273393.2:p.Gly1026Cys
NM_001199096.2:c.2917G>T	NP_001186025.1:p.Gly973Cys
NM_003933.5:c.3130G>T	NP_003924.2:p.Gly1044Cys