Canonical Allele Identifier: CA376488928

Gene: PDSS1

Linked Data

• MyVariant Identifiers: chr10:g.26986719G>C (hg19) ; chr10:g.26697790G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697790G>C , CM000672.2:g.26697790G>C	GRCh38
NC_000010.10:g.26986719G>C , CM000672.1:g.26986719G>C	GRCh37
NC_000010.9:g.27026725G>C	NCBI36
NG_008972.1:g.5125G>C
NG_008972.2:g.5125G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.79G>C MANE Select	ENSP00000365388.5:p.Gly27Arg
ENST00000376215.9:c.79G>C	ENSP00000365388.5:p.Gly27Arg
NM_014317.3:c.79G>C	NP_055132.2:p.Gly27Arg
XR_428636.2:n.367G>C
XR_930486.1:n.367G>C
NM_001321978.1:c.79G>C	NP_001308907.1:p.Gly27Arg
NM_001321979.1:c.-515G>C	NP_001308908.1:n.-515G>C
NM_014317.4:c.79G>C	NP_055132.2:p.Gly27Arg
XM_024447922.1:c.79G>C	XP_024303690.1:p.Gly27Arg
XR_428636.4:n.367G>C
NM_014317.5:c.79G>C MANE Select	NP_055132.2:p.Gly27Arg
NM_001321978.2:c.79G>C	NP_001308907.1:p.Gly27Arg
NM_001321979.2:c.-515G>C	NP_001308908.1:n.-515G>C