Canonical Allele Identifier: CA2608595070
Gene: PDSS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697947_26697956dup , CM000672.2:g.26697947_26697956dup GRCh38
NC_000010.10:g.26986876_26986885dup , CM000672.1:g.26986876_26986885dup GRCh37
NC_000010.9:g.27026882_27026891dup NCBI36
NG_008972.1:g.5282_5291dup
NG_008972.2:g.5282_5291dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.129+107_129+116dup MANE Select ENSP00000365388.5:n.129+107_129+116dup
ENST00000376215.9:c.129+107_129+116dup ENSP00000365388.5:n.129+107_129+116dup
NM_014317.3:c.129+107_129+116dup NP_055132.2:n.129+107_129+116dup
XR_428636.2:n.417+107_417+116dup
XR_930486.1:n.417+107_417+116dup
NM_001321978.1:c.129+107_129+116dup NP_001308907.1:n.129+107_129+116dup
NM_001321979.1:c.-465+107_-465+116dup NP_001308908.1:n.-465+107_-465+116dup
NM_014317.4:c.129+107_129+116dup NP_055132.2:n.129+107_129+116dup
XM_024447922.1:c.129+107_129+116dup XP_024303690.1:n.129+107_129+116dup
XR_428636.4:n.417+107_417+116dup
NM_014317.5:c.129+107_129+116dup MANE Select NP_055132.2:n.129+107_129+116dup
NM_001321978.2:c.129+107_129+116dup NP_001308907.1:n.129+107_129+116dup
NM_001321979.2:c.-465+107_-465+116dup NP_001308908.1:n.-465+107_-465+116dup