Canonical Allele Identifier: CA1868206558

Gene: BAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362726A= , CM000671.2:g.101362726A=	GRCh38
NC_000009.11:g.104125008A= , CM000671.1:g.104125008A=	GRCh37
NC_000009.10:g.103164829A=	NCBI36
NG_009774.1:g.27280T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000259407.7:c.959T= MANE Select	ENSP00000259407.2:p.Phe320=
ENST00000395051.4:c.959T=	ENSP00000378491.3:p.Phe320=
ENST00000674556.1:c.959T=	ENSP00000501610.1:p.Phe320=
ENST00000674791.1:c.762+197T=	ENSP00000501644.1:n.762+197T=
ENST00000674909.1:c.804+155T=	ENSP00000502812.1:n.804+155T=
ENST00000259407.6:c.959T=	ENSP00000259407.2:p.Phe320=
ENST00000395051.3:c.959T=	ENSP00000378491.3:p.Phe320=
NM_001127610.1:c.959T=	NP_001121082.1:p.Phe320=
NM_001701.3:c.959T=	NP_001692.1:p.Phe320=
NM_001127610.2:c.959T=	NP_001121082.1:p.Phe320=
NM_001374715.1:c.959T=	NP_001361644.1:p.Phe320=
NM_001701.4:c.959T= MANE Select	NP_001692.1:p.Phe320=