Canonical Allele Identifier: CA374254527
Gene: BAAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101362726A>G , CM000671.2:g.101362726A>G GRCh38
NC_000009.11:g.104125008A>G , CM000671.1:g.104125008A>G GRCh37
NC_000009.10:g.103164829A>G NCBI36
NG_009774.1:g.27280T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259407.7:c.959T>C MANE Select ENSP00000259407.2:p.Phe320Ser
ENST00000395051.4:c.959T>C ENSP00000378491.3:p.Phe320Ser
ENST00000674556.1:c.959T>C ENSP00000501610.1:p.Phe320Ser
ENST00000674791.1:c.762+197T>C ENSP00000501644.1:n.762+197T>C
ENST00000674909.1:c.804+155T>C ENSP00000502812.1:n.804+155T>C
ENST00000259407.6:c.959T>C ENSP00000259407.2:p.Phe320Ser
ENST00000395051.3:c.959T>C ENSP00000378491.3:p.Phe320Ser
NM_001127610.1:c.959T>C NP_001121082.1:p.Phe320Ser
NM_001701.3:c.959T>C NP_001692.1:p.Phe320Ser
NM_001127610.2:c.959T>C NP_001121082.1:p.Phe320Ser
NM_001374715.1:c.959T>C NP_001361644.1:p.Phe320Ser
NM_001701.4:c.959T>C MANE Select NP_001692.1:p.Phe320Ser