Canonical Allele Identifier: CA394164339

Gene: BAIAP3

Linked Data

• MyVariant Identifiers: chr16:g.1392736G>C (hg19) ; chr16:g.1342735G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342735G>C , CM000678.2:g.1342735G>C	GRCh38
NC_000016.9:g.1392736G>C , CM000678.1:g.1392736G>C	GRCh37
NC_000016.8:g.1332737G>C	NCBI36
NG_033974.1:g.14131G>C
NG_033974.2:g.14131G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.351G>C
ENST00000564213.2:c.1082G>C	ENSP00000518583.1:p.Ser361Thr
ENST00000565665.6:n.1455G>C
ENST00000567203.2:n.1197G>C
ENST00000711102.1:c.1082G>C	ENSP00000518580.1:p.Ser361Thr
ENST00000711103.1:c.1082G>C	ENSP00000518581.1:p.Ser361Thr
ENST00000711104.1:c.1133G>C	ENSP00000518582.1:p.Ser378Thr
ENST00000711105.1:c.1082G>C	ENSP00000518584.1:p.Ser361Thr
ENST00000711111.1:n.1198G>C
ENST00000426824.8:c.1082G>C MANE Select	ENSP00000407242.4:p.Ser361Thr
ENST00000324385.9:c.1187G>C	ENSP00000324510.5:p.Ser396Thr
ENST00000397488.6:c.1133G>C	ENSP00000380625.2:p.Ser378Thr
ENST00000421665.6:c.974G>C	ENSP00000409533.2:p.Ser325Thr
ENST00000426824.7:c.1082G>C	ENSP00000407242.3:p.Ser361Thr
ENST00000562208.5:c.1013G>C	ENSP00000458134.1:p.Ser338Thr
ENST00000568887.5:c.998G>C	ENSP00000457644.1:p.Ser333Thr
ENST00000628027.2:c.1133G>C	ENSP00000487275.1:p.Ser378Thr
NM_001199096.1:c.974G>C	NP_001186025.1:p.Ser325Thr
NM_001199097.1:c.1082G>C	NP_001186026.1:p.Ser361Thr
NM_001199098.1:c.1013G>C	NP_001186027.1:p.Ser338Thr
NM_001199099.1:c.998G>C	NP_001186028.1:p.Ser333Thr
NM_001286464.1:c.1133G>C	NP_001273393.1:p.Ser378Thr
NM_003933.4:c.1187G>C	NP_003924.2:p.Ser396Thr
XM_011522728.1:c.1238G>C	XP_011521030.1:p.Ser413Thr
XM_011522729.1:c.1238G>C	XP_011521031.1:p.Ser413Thr
XM_011522730.1:c.1238G>C	XP_011521032.1:p.Ser413Thr
XM_011522730.2:c.1238G>C	XP_011521032.1:p.Ser413Thr
NM_001199097.2:c.1082G>C MANE Select	NP_001186026.1:p.Ser361Thr
NM_001199098.2:c.1013G>C	NP_001186027.1:p.Ser338Thr
NM_001199099.2:c.998G>C	NP_001186028.1:p.Ser333Thr
NM_001286464.2:c.1133G>C	NP_001273393.2:p.Ser378Thr
NM_001199096.2:c.974G>C	NP_001186025.1:p.Ser325Thr
NM_003933.5:c.1187G>C	NP_003924.2:p.Ser396Thr