Canonical Allele Identifier: CA123059
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 13364
ClinVar RCV Id: RCV000014292
dbSNP Id: rs121918105
MyVariant Identifiers: chr10:g.73579518C>A (hg19) chr10:g.71819761C>A (hg38)
PubMed: PMID:2060627 PMID:3024666
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71819761C>A , CM000672.2:g.71819761C>A GRCh38
NC_000010.10:g.73579518C>A , CM000672.1:g.73579518C>A GRCh37
NC_000010.9:g.73249524C>A NCBI36
NG_009301.1:g.36565G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394936.8:c.1145G>T MANE Select ENSP00000378394.3:p.Cys382Phe
ENST00000394934.4:c.1154G>T ENSP00000378392.2:p.Cys385Phe
ENST00000394936.7:c.1145G>T ENSP00000378394.3:p.Cys382Phe
ENST00000493143.1:n.566G>T
ENST00000610929.3:c.293G>T ENSP00000480857.1:p.Cys98Phe
NM_001042465.1:c.1154G>T NP_001035930.1:p.Cys385Phe
NM_001042466.1:c.1151G>T NP_001035931.1:p.Cys384Phe
NM_002778.2:c.1145G>T NP_002769.1:p.Cys382Phe
NM_001042465.2:c.1154G>T NP_001035930.1:p.Cys385Phe
NM_001042466.2:c.1151G>T NP_001035931.1:p.Cys384Phe
NM_002778.3:c.1145G>T NP_002769.1:p.Cys382Phe
NM_002778.4:c.1145G>T MANE Select NP_002769.1:p.Cys382Phe
NM_001042465.3:c.1154G>T NP_001035930.1:p.Cys385Phe
NM_001042466.3:c.1151G>T NP_001035931.1:p.Cys384Phe
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