Canonical Allele Identifier: CA470061813

Gene: PSAP

Linked Data

• MyVariant Identifiers: chr10:g.73594132T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71834375T>A , CM000672.2:g.71834375T>A	GRCh38
NC_000010.10:g.73594132T>A , CM000672.1:g.73594132T>A	GRCh37
NC_000010.9:g.73264138T>A	NCBI36
NG_009301.1:g.21951A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394936.8:c.171A>T MANE Select	ENSP00000378394.3:p.Thr57=
ENST00000394934.4:c.171A>T	ENSP00000378392.2:p.Thr57=
ENST00000394936.7:c.171A>T	ENSP00000378394.3:p.Thr57=
ENST00000610929.3:c.171A>T	ENSP00000480857.1:p.Thr57=
NM_001042465.1:c.171A>T	NP_001035930.1:p.Thr57=
NM_001042466.1:c.171A>T	NP_001035931.1:p.Thr57=
NM_002778.2:c.171A>T	NP_002769.1:p.Thr57=
NM_001042465.2:c.171A>T	NP_001035930.1:p.Thr57=
NM_001042466.2:c.171A>T	NP_001035931.1:p.Thr57=
NM_002778.3:c.171A>T	NP_002769.1:p.Thr57=
NM_002778.4:c.171A>T MANE Select	NP_002769.1:p.Thr57=
NM_001042465.3:c.171A>T	NP_001035930.1:p.Thr57=
NM_001042466.3:c.171A>T	NP_001035931.1:p.Thr57=