Canonical Allele Identifier: CA663313133

Gene: PDSS1

Linked Data

• dbSNP Id: rs1441324216
• gnomAD v3: 10-26710004-AT-A
• gnomAD v4: 10-26710004-AT-A
• MyVariant Identifiers: chr10:g.26998934del (hg19) ; chr10:g.26710005del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26710006del , CM000672.2:g.26710006del	GRCh38
NC_000010.10:g.26998935del , CM000672.1:g.26998935del	GRCh37
NC_000010.9:g.27038941del	NCBI36
NG_008972.1:g.17341del
NG_008972.2:g.17341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.467+238del MANE Select	ENSP00000365388.5:n.467+238del
ENST00000376215.9:c.467+238del	ENSP00000365388.5:n.467+238del
ENST00000473224.1:n.218+238del
NM_014317.3:c.467+238del	NP_055132.2:n.467+238del
XM_005252439.2:c.-127+238del	XP_005252496.1:n.-127+238del
XM_011519437.1:c.98+238del	XP_011517739.1:n.98+238del
XR_428636.2:n.755+238del
XR_930486.1:n.755+238del
NM_001321978.1:c.467+238del	NP_001308907.1:n.467+238del
NM_001321979.1:c.-127+238del	NP_001308908.1:n.-127+238del
NM_014317.4:c.467+238del	NP_055132.2:n.467+238del
XM_011519437.3:c.98+238del	XP_011517739.1:n.98+238del
XM_017016011.2:c.146+238del	XP_016871500.1:n.146+238del
XM_024447922.1:c.467+238del	XP_024303690.1:n.467+238del
XM_024447923.1:c.-127+238del	XP_024303691.1:n.-127+238del
XR_428636.4:n.755+238del
NM_014317.5:c.467+238del MANE Select	NP_055132.2:n.467+238del
NM_001321978.2:c.467+238del	NP_001308907.1:n.467+238del
NM_001321979.2:c.-127+238del	NP_001308908.1:n.-127+238del