Canonical Allele Identifier: CA374254299
Gene: BAAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101362619A>G , CM000671.2:g.101362619A>G GRCh38
NC_000009.11:g.104124901A>G , CM000671.1:g.104124901A>G GRCh37
NC_000009.10:g.103164722A>G NCBI36
NG_009774.1:g.27387T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259407.7:c.1066T>C MANE Select ENSP00000259407.2:p.Ser356Pro
ENST00000395051.4:c.1066T>C ENSP00000378491.3:p.Ser356Pro
ENST00000674556.1:c.1066T>C ENSP00000501610.1:p.Ser356Pro
ENST00000674791.1:c.762+304T>C ENSP00000501644.1:n.762+304T>C
ENST00000674909.1:c.804+262T>C ENSP00000502812.1:n.804+262T>C
ENST00000259407.6:c.1066T>C ENSP00000259407.2:p.Ser356Pro
ENST00000395051.3:c.1066T>C ENSP00000378491.3:p.Ser356Pro
NM_001127610.1:c.1066T>C NP_001121082.1:p.Ser356Pro
NM_001701.3:c.1066T>C NP_001692.1:p.Ser356Pro
NM_001127610.2:c.1066T>C NP_001121082.1:p.Ser356Pro
NM_001374715.1:c.1066T>C NP_001361644.1:p.Ser356Pro
NM_001701.4:c.1066T>C MANE Select NP_001692.1:p.Ser356Pro