Canonical Allele Identifier: CA1868206675

Gene: BAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362792G= , CM000671.2:g.101362792G=	GRCh38
NC_000009.11:g.104125074G= , CM000671.1:g.104125074G=	GRCh37
NC_000009.10:g.103164895G=	NCBI36
NG_009774.1:g.27214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259407.7:c.893C= MANE Select	ENSP00000259407.2:p.Thr298=
ENST00000395051.4:c.893C=	ENSP00000378491.3:p.Thr298=
ENST00000674556.1:c.893C=	ENSP00000501610.1:p.Thr298=
ENST00000674791.1:c.762+131C=	ENSP00000501644.1:n.762+131C=
ENST00000674909.1:c.804+89C=	ENSP00000502812.1:n.804+89C=
ENST00000259407.6:c.893C=	ENSP00000259407.2:p.Thr298=
ENST00000395051.3:c.893C=	ENSP00000378491.3:p.Thr298=
NM_001127610.1:c.893C=	NP_001121082.1:p.Thr298=
NM_001701.3:c.893C=	NP_001692.1:p.Thr298=
NM_001127610.2:c.893C=	NP_001121082.1:p.Thr298=
NM_001374715.1:c.893C=	NP_001361644.1:p.Thr298=
NM_001701.4:c.893C= MANE Select	NP_001692.1:p.Thr298=