Canonical Allele Identifier: CA394164354

Gene: BAIAP3

Linked Data

• MyVariant Identifiers: chr16:g.1392739A>T (hg19) ; chr16:g.1342738A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1342738A>T , CM000678.2:g.1342738A>T	GRCh38
NC_000016.9:g.1392739A>T , CM000678.1:g.1392739A>T	GRCh37
NC_000016.8:g.1332740A>T	NCBI36
NG_033974.1:g.14134A>T
NG_033974.2:g.14134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561793.2:c.354A>T
ENST00000564213.2:c.1085A>T	ENSP00000518583.1:p.Gln362Leu
ENST00000565665.6:n.1458A>T
ENST00000567203.2:n.1200A>T
ENST00000711102.1:c.1085A>T	ENSP00000518580.1:p.Gln362Leu
ENST00000711103.1:c.1085A>T	ENSP00000518581.1:p.Gln362Leu
ENST00000711104.1:c.1136A>T	ENSP00000518582.1:p.Gln379Leu
ENST00000711105.1:c.1085A>T	ENSP00000518584.1:p.Gln362Leu
ENST00000711111.1:n.1201A>T
ENST00000426824.8:c.1085A>T MANE Select	ENSP00000407242.4:p.Gln362Leu
ENST00000324385.9:c.1190A>T	ENSP00000324510.5:p.Gln397Leu
ENST00000397488.6:c.1136A>T	ENSP00000380625.2:p.Gln379Leu
ENST00000421665.6:c.977A>T	ENSP00000409533.2:p.Gln326Leu
ENST00000426824.7:c.1085A>T	ENSP00000407242.3:p.Gln362Leu
ENST00000562208.5:c.1016A>T	ENSP00000458134.1:p.Gln339Leu
ENST00000568887.5:c.1001A>T	ENSP00000457644.1:p.Gln334Leu
ENST00000628027.2:c.1136A>T	ENSP00000487275.1:p.Gln379Leu
NM_001199096.1:c.977A>T	NP_001186025.1:p.Gln326Leu
NM_001199097.1:c.1085A>T	NP_001186026.1:p.Gln362Leu
NM_001199098.1:c.1016A>T	NP_001186027.1:p.Gln339Leu
NM_001199099.1:c.1001A>T	NP_001186028.1:p.Gln334Leu
NM_001286464.1:c.1136A>T	NP_001273393.1:p.Gln379Leu
NM_003933.4:c.1190A>T	NP_003924.2:p.Gln397Leu
XM_011522728.1:c.1241A>T	XP_011521030.1:p.Gln414Leu
XM_011522729.1:c.1241A>T	XP_011521031.1:p.Gln414Leu
XM_011522730.1:c.1241A>T	XP_011521032.1:p.Gln414Leu
XM_011522730.2:c.1241A>T	XP_011521032.1:p.Gln414Leu
NM_001199097.2:c.1085A>T MANE Select	NP_001186026.1:p.Gln362Leu
NM_001199098.2:c.1016A>T	NP_001186027.1:p.Gln339Leu
NM_001199099.2:c.1001A>T	NP_001186028.1:p.Gln334Leu
NM_001286464.2:c.1136A>T	NP_001273393.2:p.Gln379Leu
NM_001199096.2:c.977A>T	NP_001186025.1:p.Gln326Leu
NM_003933.5:c.1190A>T	NP_003924.2:p.Gln397Leu