Canonical Allele Identifier: CA466650540

Gene: BAAT

Linked Data

• MyVariant Identifiers: chr9:g.104124920C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362638C>T , CM000671.2:g.101362638C>T	GRCh38
NC_000009.11:g.104124920C>T , CM000671.1:g.104124920C>T	GRCh37
NC_000009.10:g.103164741C>T	NCBI36
NG_009774.1:g.27368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259407.7:c.1047G>A MANE Select	ENSP00000259407.2:p.Lys349=
ENST00000395051.4:c.1047G>A	ENSP00000378491.3:p.Lys349=
ENST00000674556.1:c.1047G>A	ENSP00000501610.1:p.Lys349=
ENST00000674791.1:c.762+285G>A	ENSP00000501644.1:n.762+285G>A
ENST00000674909.1:c.804+243G>A	ENSP00000502812.1:n.804+243G>A
ENST00000259407.6:c.1047G>A	ENSP00000259407.2:p.Lys349=
ENST00000395051.3:c.1047G>A	ENSP00000378491.3:p.Lys349=
NM_001127610.1:c.1047G>A	NP_001121082.1:p.Lys349=
NM_001701.3:c.1047G>A	NP_001692.1:p.Lys349=
NM_001127610.2:c.1047G>A	NP_001121082.1:p.Lys349=
NM_001374715.1:c.1047G>A	NP_001361644.1:p.Lys349=
NM_001701.4:c.1047G>A MANE Select	NP_001692.1:p.Lys349=