Canonical Allele Identifier: CA1857665734

Gene: PSAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304854C= , CM000671.2:g.78304854C=	GRCh38
NC_000009.11:g.80919770C= , CM000671.1:g.80919770C=	GRCh37
NC_000009.10:g.80109590C=	NCBI36
NG_012165.1:g.12712C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.311C= MANE Select	ENSP00000365773.3:p.Thr104=
ENST00000347159.6:c.311C=	ENSP00000317606.2:p.Thr104=
ENST00000376588.3:c.311C=	ENSP00000365773.3:p.Thr104=
NM_021154.4:c.311C=	NP_066977.1:p.Thr104=
NM_058179.3:c.311C=	NP_478059.1:p.Thr104=
NM_058179.4:c.311C= MANE Select	NP_478059.1:p.Thr104=
NM_021154.5:c.311C=	NP_066977.1:p.Thr104=