Canonical Allele Identifier: CA1857677065
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329869C= , CM000671.2:g.78329869C= GRCh38
NC_000009.11:g.80944785C= , CM000671.1:g.80944785C= GRCh37
NC_000009.10:g.80134605C= NCBI36
NG_012165.1:g.37727C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*783C= MANE Select ENSP00000365773.3:n.*783C=
ENST00000376588.3:c.*783C= ENSP00000365773.3:n.*783C=
NM_021154.4:c.*783C= NP_066977.1:n.*783C=
NM_058179.3:c.*783C= NP_478059.1:n.*783C=
NM_058179.4:c.*783C= MANE Select NP_478059.1:n.*783C=
NM_021154.5:c.*783C= NP_066977.1:n.*783C=
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