Canonical Allele Identifier: CA620700008

Gene: BAIAP3

Linked Data

• dbSNP Id: rs1435241526
• gnomAD v2: 16-1397829-T-C
• gnomAD v3: 16-1347828-T-C
• gnomAD v4: 16-1347828-T-C
• MyVariant Identifiers: chr16:g.1397829T>C (hg19) ; chr16:g.1347828T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1347828T>C , CM000678.2:g.1347828T>C	GRCh38
NC_000016.9:g.1397829T>C , CM000678.1:g.1397829T>C	GRCh37
NC_000016.8:g.1337830T>C	NCBI36
NG_016985.1:g.930T>C
NG_033974.1:g.19224T>C
NG_033974.2:g.19224T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000561793.2:c.2207+7T>C
ENST00000564213.2:c.*219+7T>C	ENSP00000518583.1:n.*219+7T>C
ENST00000565665.6:n.3289+7T>C
ENST00000567203.2:n.3644+7T>C
ENST00000568198.2:n.1806+7T>C
ENST00000711102.1:c.3025+7T>C	ENSP00000518580.1:n.3025+7T>C
ENST00000711103.1:c.*1208+7T>C	ENSP00000518581.1:n.*1208+7T>C
ENST00000711104.1:c.*219+7T>C	ENSP00000518582.1:n.*219+7T>C
ENST00000711105.1:c.2962+7T>C	ENSP00000518584.1:n.2962+7T>C
ENST00000711106.1:c.1684+7T>C	ENSP00000518585.1:n.1684+7T>C
ENST00000711107.1:c.1621+7T>C	ENSP00000518586.1:n.1621+7T>C
ENST00000711108.1:c.1684+7T>C	ENSP00000518587.1:n.1684+7T>C
ENST00000711109.1:c.*1066+7T>C	ENSP00000518588.1:n.*1066+7T>C
ENST00000711110.1:c.343+7T>C	ENSP00000518589.1:n.343+7T>C
ENST00000711111.1:n.3367+7T>C
ENST00000426824.8:c.3025+7T>C MANE Select	ENSP00000407242.4:n.3025+7T>C
ENST00000324385.9:c.3130+7T>C	ENSP00000324510.5:n.3130+7T>C
ENST00000397488.6:c.3076+7T>C	ENSP00000380625.2:n.3076+7T>C
ENST00000421665.6:c.2917+7T>C	ENSP00000409533.2:n.2917+7T>C
ENST00000426824.7:c.3025+7T>C	ENSP00000407242.3:n.3025+7T>C
ENST00000562208.5:c.2956+7T>C	ENSP00000458134.1:n.2956+7T>C
ENST00000566162.1:c.627-1538T>C
ENST00000566389.1:n.511+7T>C
ENST00000568887.5:c.2941+7T>C	ENSP00000457644.1:n.2941+7T>C
ENST00000628027.2:c.3076+7T>C	ENSP00000487275.1:n.3076+7T>C
NM_001199096.1:c.2917+7T>C	NP_001186025.1:n.2917+7T>C
NM_001199097.1:c.3025+7T>C	NP_001186026.1:n.3025+7T>C
NM_001199098.1:c.2956+7T>C	NP_001186027.1:n.2956+7T>C
NM_001199099.1:c.2941+7T>C	NP_001186028.1:n.2941+7T>C
NM_001286464.1:c.3076+7T>C	NP_001273393.1:n.3076+7T>C
NM_003933.4:c.3130+7T>C	NP_003924.2:n.3130+7T>C
XM_011522728.1:c.3181+7T>C	XP_011521030.1:n.3181+7T>C
XM_011522729.1:c.3181+7T>C	XP_011521031.1:n.3181+7T>C
XM_011522730.1:c.3181+7T>C	XP_011521032.1:n.3181+7T>C
XM_011522730.2:c.3181+7T>C	XP_011521032.1:n.3181+7T>C
NM_001199097.2:c.3025+7T>C MANE Select	NP_001186026.1:n.3025+7T>C
NM_001199098.2:c.2956+7T>C	NP_001186027.1:n.2956+7T>C
NM_001199099.2:c.2941+7T>C	NP_001186028.1:n.2941+7T>C
NM_001286464.2:c.3076+7T>C	NP_001273393.2:n.3076+7T>C
NM_001199096.2:c.2917+7T>C	NP_001186025.1:n.2917+7T>C
NM_003933.5:c.3130+7T>C	NP_003924.2:n.3130+7T>C