Canonical Allele Identifier: CA2160932454
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741273_104741274delinsAC , CM000676.2:g.104741273_104741274delinsAC GRCh38
NC_000014.8:g.105207610_105207611delinsAC , CM000676.1:g.105207610_105207611delinsAC GRCh37
NC_000014.7:g.104278655_104278656delinsAC NCBI36
NG_051175.1:g.22077_22078delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710323.1:c.793+30_793+31delinsAC ENSP00000518203.1:n.793+30_793+31delinsAC
ENST00000330877.7:c.793+30_793+31delinsAC MANE Select ENSP00000331260.2:n.793+30_793+31delinsAC
ENST00000330877.6:c.793+30_793+31delinsAC ENSP00000331260.2:n.793+30_793+31delinsAC
ENST00000332972.9:c.922+30_922+31delinsAC ENSP00000333019.5:n.922+30_922+31delinsAC
ENST00000553540.5:c.905+30_905+31delinsAC ENSP00000450759.1:n.905+30_905+31delinsAC
ENST00000555486.5:c.858+30_858+31delinsAC ENSP00000473778.1:n.858+30_858+31delinsAC
ENST00000557582.5:n.1714+30_1714+31delinsAC
NM_152328.3:c.793+30_793+31delinsAC NP_689541.1:n.793+30_793+31delinsAC
NM_199165.1:c.922+30_922+31delinsAC NP_954634.1:n.922+30_922+31delinsAC
XM_006720026.2:c.796+30_796+31delinsAC XP_006720089.1:n.796+30_796+31delinsAC
XM_011536412.1:c.925+30_925+31delinsAC XP_011534714.1:n.925+30_925+31delinsAC
XM_011536413.1:c.610+30_610+31delinsAC XP_011534715.1:n.610+30_610+31delinsAC
XM_011536414.1:c.607+30_607+31delinsAC XP_011534716.1:n.607+30_607+31delinsAC
XM_011536415.1:c.178+30_178+31delinsAC XP_011534717.1:n.178+30_178+31delinsAC
NM_001320424.1:c.178+30_178+31delinsAC NP_001307353.1:n.178+30_178+31delinsAC
NM_152328.4:c.793+30_793+31delinsAC NP_689541.1:n.793+30_793+31delinsAC
NM_199165.2:c.922+30_922+31delinsAC NP_954634.1:n.922+30_922+31delinsAC
XM_006720026.3:c.796+30_796+31delinsAC XP_006720089.1:n.796+30_796+31delinsAC
XM_011536412.2:c.925+30_925+31delinsAC XP_011534714.1:n.925+30_925+31delinsAC
XR_001750917.1:n.435_436delinsGT
NM_152328.5:c.793+30_793+31delinsAC MANE Select NP_689541.1:n.793+30_793+31delinsAC