Canonical Allele Identifier: CA594309265

Gene: PSAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71823922G>T , CM000672.2:g.71823922G>T	GRCh38
NC_000010.10:g.73583679G>T , CM000672.1:g.73583679G>T	GRCh37
NC_000010.9:g.73253685G>T	NCBI36
NG_009301.1:g.32404C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002778.4:c.778-1915C>A MANE Select	NP_002769.1:n.778-1915C>A
ENST00000394936.8:c.778-1915C>A MANE Select	ENSP00000378394.3:n.778-1915C>A
NM_001042465.1:c.778-26C>A	NP_001035930.1:n.778-26C>A
NM_001042465.2:c.778-26C>A	NP_001035930.1:n.778-26C>A
NM_001042465.3:c.778-26C>A	NP_001035930.1:n.778-26C>A
NM_001042466.1:c.778-29C>A	NP_001035931.1:n.778-29C>A
NM_001042466.2:c.778-29C>A	NP_001035931.1:n.778-29C>A
NM_001042466.3:c.778-29C>A	NP_001035931.1:n.778-29C>A
NM_002778.2:c.778-1915C>A	NP_002769.1:n.778-1915C>A
NM_002778.3:c.778-1915C>A	NP_002769.1:n.778-1915C>A
ENST00000394934.4:c.778-1906C>A	ENSP00000378392.2:n.778-1906C>A
ENST00000394936.7:c.778-1915C>A	ENSP00000378394.3:n.778-1915C>A
ENST00000610929.3:c.271-4139C>A	ENSP00000480857.1:n.271-4139C>A
ENST00000633965.1:c.179-26C>A