Canonical Allele Identifier: CA1857677073
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329885_78329886delinsGA , CM000671.2:g.78329885_78329886delinsGA GRCh38
NC_000009.11:g.80944801_80944802delinsGA , CM000671.1:g.80944801_80944802delinsGA GRCh37
NC_000009.10:g.80134621_80134622delinsGA NCBI36
NG_012165.1:g.37743_37744delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*799_*800delinsGA MANE Select ENSP00000365773.3:n.*799_*800delinsGA
ENST00000376588.3:c.*799_*800delinsGA ENSP00000365773.3:n.*799_*800delinsGA
NM_021154.4:c.*799_*800delinsGA NP_066977.1:n.*799_*800delinsGA
NM_058179.3:c.*799_*800delinsGA NP_478059.1:n.*799_*800delinsGA
NM_058179.4:c.*799_*800delinsGA MANE Select NP_478059.1:n.*799_*800delinsGA
NM_021154.5:c.*799_*800delinsGA NP_066977.1:n.*799_*800delinsGA
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