Canonical Allele Identifier: CA2843083340
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741278dup , CM000676.2:g.104741278dup GRCh38
NC_000014.8:g.105207615dup , CM000676.1:g.105207615dup GRCh37
NC_000014.7:g.104278660dup NCBI36
NG_051175.1:g.22082dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710323.1:c.793+35dup ENSP00000518203.1:n.793+35dup
ENST00000330877.7:c.793+35dup MANE Select ENSP00000331260.2:n.793+35dup
ENST00000330877.6:c.793+35dup ENSP00000331260.2:n.793+35dup
ENST00000332972.9:c.922+35dup ENSP00000333019.5:n.922+35dup
ENST00000553540.5:c.905+35dup ENSP00000450759.1:n.905+35dup
ENST00000555486.5:c.858+35dup ENSP00000473778.1:n.858+35dup
ENST00000557582.5:n.1714+35dup
NM_152328.3:c.793+35dup NP_689541.1:n.793+35dup
NM_199165.1:c.922+35dup NP_954634.1:n.922+35dup
XM_006720026.2:c.796+35dup XP_006720089.1:n.796+35dup
XM_011536412.1:c.925+35dup XP_011534714.1:n.925+35dup
XM_011536413.1:c.610+35dup XP_011534715.1:n.610+35dup
XM_011536414.1:c.607+35dup XP_011534716.1:n.607+35dup
XM_011536415.1:c.178+35dup XP_011534717.1:n.178+35dup
NM_001320424.1:c.178+35dup NP_001307353.1:n.178+35dup
NM_152328.4:c.793+35dup NP_689541.1:n.793+35dup
NM_199165.2:c.922+35dup NP_954634.1:n.922+35dup
XM_006720026.3:c.796+35dup XP_006720089.1:n.796+35dup
XM_011536412.2:c.925+35dup XP_011534714.1:n.925+35dup
XR_001750917.1:n.433dup
NM_152328.5:c.793+35dup MANE Select NP_689541.1:n.793+35dup