Canonical Allele Identifier: CA205006624

Gene: PDSS1

Linked Data

• dbSNP Id: rs886046933
• MyVariant Identifiers: chr10:g.26986737G>C (hg19) ; chr10:g.26697808G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697808G>C , CM000672.2:g.26697808G>C	GRCh38
NC_000010.10:g.26986737G>C , CM000672.1:g.26986737G>C	GRCh37
NC_000010.9:g.27026743G>C	NCBI36
NG_008972.1:g.5143G>C
NG_008972.2:g.5143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.97G>C MANE Select	ENSP00000365388.5:p.Gly33Arg
ENST00000376215.9:c.97G>C	ENSP00000365388.5:p.Gly33Arg
NM_014317.3:c.97G>C	NP_055132.2:p.Gly33Arg
XR_428636.2:n.385G>C
XR_930486.1:n.385G>C
NM_001321978.1:c.97G>C	NP_001308907.1:p.Gly33Arg
NM_001321979.1:c.-497G>C	NP_001308908.1:n.-497G>C
NM_014317.4:c.97G>C	NP_055132.2:p.Gly33Arg
XM_024447922.1:c.97G>C	XP_024303690.1:p.Gly33Arg
XR_428636.4:n.385G>C
NM_014317.5:c.97G>C MANE Select	NP_055132.2:p.Gly33Arg
NM_001321978.2:c.97G>C	NP_001308907.1:p.Gly33Arg
NM_001321979.2:c.-497G>C	NP_001308908.1:n.-497G>C