Canonical Allele Identifier: CA466650607

Gene: BAAT

Linked Data

• MyVariant Identifiers: chr9:g.104125076G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101362794G>C , CM000671.2:g.101362794G>C	GRCh38
NC_000009.11:g.104125076G>C , CM000671.1:g.104125076G>C	GRCh37
NC_000009.10:g.103164897G>C	NCBI36
NG_009774.1:g.27212C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259407.7:c.891C>G MANE Select	ENSP00000259407.2:p.Arg297=
ENST00000395051.4:c.891C>G	ENSP00000378491.3:p.Arg297=
ENST00000674556.1:c.891C>G	ENSP00000501610.1:p.Arg297=
ENST00000674791.1:c.762+129C>G	ENSP00000501644.1:n.762+129C>G
ENST00000674909.1:c.804+87C>G	ENSP00000502812.1:n.804+87C>G
ENST00000259407.6:c.891C>G	ENSP00000259407.2:p.Arg297=
ENST00000395051.3:c.891C>G	ENSP00000378491.3:p.Arg297=
NM_001127610.1:c.891C>G	NP_001121082.1:p.Arg297=
NM_001701.3:c.891C>G	NP_001692.1:p.Arg297=
NM_001127610.2:c.891C>G	NP_001121082.1:p.Arg297=
NM_001374715.1:c.891C>G	NP_001361644.1:p.Arg297=
NM_001701.4:c.891C>G MANE Select	NP_001692.1:p.Arg297=