Canonical Allele Identifier: CA1918891186

Gene: PSAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71834499G= , CM000672.2:g.71834499G=	GRCh38
NC_000010.10:g.73594256G= , CM000672.1:g.73594256G=	GRCh37
NC_000010.9:g.73264262G=	NCBI36
NG_009301.1:g.21827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394936.8:c.47C= MANE Select	ENSP00000378394.3:p.Ala16=
ENST00000394934.4:c.47C=	ENSP00000378392.2:p.Ala16=
ENST00000394936.7:c.47C=	ENSP00000378394.3:p.Ala16=
ENST00000610929.3:c.47C=	ENSP00000480857.1:p.Ala16=
NM_001042465.1:c.47C=	NP_001035930.1:p.Ala16=
NM_001042466.1:c.47C=	NP_001035931.1:p.Ala16=
NM_002778.2:c.47C=	NP_002769.1:p.Ala16=
NM_001042465.2:c.47C=	NP_001035930.1:p.Ala16=
NM_001042466.2:c.47C=	NP_001035931.1:p.Ala16=
NM_002778.3:c.47C=	NP_002769.1:p.Ala16=
NM_002778.4:c.47C= MANE Select	NP_002769.1:p.Ala16=
NM_001042465.3:c.47C=	NP_001035930.1:p.Ala16=
NM_001042466.3:c.47C=	NP_001035931.1:p.Ala16=