Canonical Allele Identifier: CA468624836

Gene: PDSS1

Linked Data

• dbSNP Id: rs1834912984
• gnomAD v3: 10-26697805-T-C
• gnomAD v4: 10-26697805-T-C
• MyVariant Identifiers: chr10:g.26986734T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697805T>C , CM000672.2:g.26697805T>C	GRCh38
NC_000010.10:g.26986734T>C , CM000672.1:g.26986734T>C	GRCh37
NC_000010.9:g.27026740T>C	NCBI36
NG_008972.1:g.5140T>C
NG_008972.2:g.5140T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.94T>C MANE Select	ENSP00000365388.5:p.Leu32=
ENST00000376215.9:c.94T>C	ENSP00000365388.5:p.Leu32=
NM_014317.3:c.94T>C	NP_055132.2:p.Leu32=
XR_428636.2:n.382T>C
XR_930486.1:n.382T>C
NM_001321978.1:c.94T>C	NP_001308907.1:p.Leu32=
NM_001321979.1:c.-500T>C	NP_001308908.1:n.-500T>C
NM_014317.4:c.94T>C	NP_055132.2:p.Leu32=
XM_024447922.1:c.94T>C	XP_024303690.1:p.Leu32=
XR_428636.4:n.382T>C
NM_014317.5:c.94T>C MANE Select	NP_055132.2:p.Leu32=
NM_001321978.2:c.94T>C	NP_001308907.1:p.Leu32=
NM_001321979.2:c.-500T>C	NP_001308908.1:n.-500T>C