Canonical Allele Identifier: CA470061823

Gene: PSAP

Linked Data

• gnomAD v4: 10-71834390-A-G
• MyVariant Identifiers: chr10:g.73594147A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71834390A>G , CM000672.2:g.71834390A>G	GRCh38
NC_000010.10:g.73594147A>G , CM000672.1:g.73594147A>G	GRCh37
NC_000010.9:g.73264153A>G	NCBI36
NG_009301.1:g.21936T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394936.8:c.156T>C MANE Select	ENSP00000378394.3:p.Val52=
ENST00000394934.4:c.156T>C	ENSP00000378392.2:p.Val52=
ENST00000394936.7:c.156T>C	ENSP00000378394.3:p.Val52=
ENST00000610929.3:c.156T>C	ENSP00000480857.1:p.Val52=
NM_001042465.1:c.156T>C	NP_001035930.1:p.Val52=
NM_001042466.1:c.156T>C	NP_001035931.1:p.Val52=
NM_002778.2:c.156T>C	NP_002769.1:p.Val52=
NM_001042465.2:c.156T>C	NP_001035930.1:p.Val52=
NM_001042466.2:c.156T>C	NP_001035931.1:p.Val52=
NM_002778.3:c.156T>C	NP_002769.1:p.Val52=
NM_002778.4:c.156T>C MANE Select	NP_002769.1:p.Val52=
NM_001042465.3:c.156T>C	NP_001035930.1:p.Val52=
NM_001042466.3:c.156T>C	NP_001035931.1:p.Val52=