Canonical Allele Identifier: CA374254517

Gene: BAAT

Linked Data

• MyVariant Identifiers: chr9:g.104125003A>T (hg19) ; chr9:g.101362721A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362721A>T , CM000671.2:g.101362721A>T	GRCh38
NC_000009.11:g.104125003A>T , CM000671.1:g.104125003A>T	GRCh37
NC_000009.10:g.103164824A>T	NCBI36
NG_009774.1:g.27285T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000259407.7:c.964T>A MANE Select	ENSP00000259407.2:p.Phe322Ile
ENST00000395051.4:c.964T>A	ENSP00000378491.3:p.Phe322Ile
ENST00000674556.1:c.964T>A	ENSP00000501610.1:p.Phe322Ile
ENST00000674791.1:c.762+202T>A	ENSP00000501644.1:n.762+202T>A
ENST00000674909.1:c.804+160T>A	ENSP00000502812.1:n.804+160T>A
ENST00000259407.6:c.964T>A	ENSP00000259407.2:p.Phe322Ile
ENST00000395051.3:c.964T>A	ENSP00000378491.3:p.Phe322Ile
NM_001127610.1:c.964T>A	NP_001121082.1:p.Phe322Ile
NM_001701.3:c.964T>A	NP_001692.1:p.Phe322Ile
NM_001127610.2:c.964T>A	NP_001121082.1:p.Phe322Ile
NM_001374715.1:c.964T>A	NP_001361644.1:p.Phe322Ile
NM_001701.4:c.964T>A MANE Select	NP_001692.1:p.Phe322Ile