Canonical Allele Identifier: CA374254512

Gene: BAAT

Linked Data

• MyVariant Identifiers: chr9:g.104125002A>C (hg19) ; chr9:g.101362720A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362720A>C , CM000671.2:g.101362720A>C	GRCh38
NC_000009.11:g.104125002A>C , CM000671.1:g.104125002A>C	GRCh37
NC_000009.10:g.103164823A>C	NCBI36
NG_009774.1:g.27286T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000259407.7:c.965T>G MANE Select	ENSP00000259407.2:p.Phe322Cys
ENST00000395051.4:c.965T>G	ENSP00000378491.3:p.Phe322Cys
ENST00000674556.1:c.965T>G	ENSP00000501610.1:p.Phe322Cys
ENST00000674791.1:c.762+203T>G	ENSP00000501644.1:n.762+203T>G
ENST00000674909.1:c.804+161T>G	ENSP00000502812.1:n.804+161T>G
ENST00000259407.6:c.965T>G	ENSP00000259407.2:p.Phe322Cys
ENST00000395051.3:c.965T>G	ENSP00000378491.3:p.Phe322Cys
NM_001127610.1:c.965T>G	NP_001121082.1:p.Phe322Cys
NM_001701.3:c.965T>G	NP_001692.1:p.Phe322Cys
NM_001127610.2:c.965T>G	NP_001121082.1:p.Phe322Cys
NM_001374715.1:c.965T>G	NP_001361644.1:p.Phe322Cys
NM_001701.4:c.965T>G MANE Select	NP_001692.1:p.Phe322Cys