Canonical Allele Identifier: CA209455674

Gene: PSAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71820239C>T , CM000672.2:g.71820239C>T	GRCh38
NC_000010.10:g.73579996C>T , CM000672.1:g.73579996C>T	GRCh37
NC_000010.9:g.73250002C>T	NCBI36
NG_009301.1:g.36087G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002778.4:c.1005+1G>A MANE Select	NP_002769.1:n.1005+1G>A
ENST00000394936.8:c.1005+1G>A MANE Select	ENSP00000378394.3:n.1005+1G>A
NM_001042465.1:c.1014+1G>A	NP_001035930.1:n.1014+1G>A
NM_001042465.2:c.1014+1G>A	NP_001035930.1:n.1014+1G>A
NM_001042465.3:c.1014+1G>A	NP_001035930.1:n.1014+1G>A
NM_001042466.1:c.1011+1G>A	NP_001035931.1:n.1011+1G>A
NM_001042466.2:c.1011+1G>A	NP_001035931.1:n.1011+1G>A
NM_001042466.3:c.1011+1G>A	NP_001035931.1:n.1011+1G>A
NM_002778.2:c.1005+1G>A	NP_002769.1:n.1005+1G>A
NM_002778.3:c.1005+1G>A	NP_002769.1:n.1005+1G>A
ENST00000394934.4:c.1014+1G>A	ENSP00000378392.2:n.1014+1G>A
ENST00000394936.7:c.1005+1G>A	ENSP00000378394.3:n.1005+1G>A
ENST00000493143.1:n.426+1G>A
ENST00000610929.3:c.271-456G>A	ENSP00000480857.1:n.271-456G>A
ENST00000633965.1:c.415+1G>A