Canonical Allele Identifier: CA374254636

Gene: BAAT

Linked Data

• MyVariant Identifiers: chr9:g.104125058T>A (hg19) ; chr9:g.101362776T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362776T>A , CM000671.2:g.101362776T>A	GRCh38
NC_000009.11:g.104125058T>A , CM000671.1:g.104125058T>A	GRCh37
NC_000009.10:g.103164879T>A	NCBI36
NG_009774.1:g.27230A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259407.7:c.909A>T MANE Select	ENSP00000259407.2:p.Gln303His
ENST00000395051.4:c.909A>T	ENSP00000378491.3:p.Gln303His
ENST00000674556.1:c.909A>T	ENSP00000501610.1:p.Gln303His
ENST00000674791.1:c.762+147A>T	ENSP00000501644.1:n.762+147A>T
ENST00000674909.1:c.804+105A>T	ENSP00000502812.1:n.804+105A>T
ENST00000259407.6:c.909A>T	ENSP00000259407.2:p.Gln303His
ENST00000395051.3:c.909A>T	ENSP00000378491.3:p.Gln303His
NM_001127610.1:c.909A>T	NP_001121082.1:p.Gln303His
NM_001701.3:c.909A>T	NP_001692.1:p.Gln303His
NM_001127610.2:c.909A>T	NP_001121082.1:p.Gln303His
NM_001374715.1:c.909A>T	NP_001361644.1:p.Gln303His
NM_001701.4:c.909A>T MANE Select	NP_001692.1:p.Gln303His