Canonical Allele Identifier: CA2843083339
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741275C>T , CM000676.2:g.104741275C>T GRCh38
NC_000014.8:g.105207612C>T , CM000676.1:g.105207612C>T GRCh37
NC_000014.7:g.104278657C>T NCBI36
NG_051175.1:g.22079C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710323.1:c.793+32C>T ENSP00000518203.1:n.793+32C>T
ENST00000330877.7:c.793+32C>T MANE Select ENSP00000331260.2:n.793+32C>T
ENST00000330877.6:c.793+32C>T ENSP00000331260.2:n.793+32C>T
ENST00000332972.9:c.922+32C>T ENSP00000333019.5:n.922+32C>T
ENST00000553540.5:c.905+32C>T ENSP00000450759.1:n.905+32C>T
ENST00000555486.5:c.858+32C>T ENSP00000473778.1:n.858+32C>T
ENST00000557582.5:n.1714+32C>T
NM_152328.3:c.793+32C>T NP_689541.1:n.793+32C>T
NM_199165.1:c.922+32C>T NP_954634.1:n.922+32C>T
XM_006720026.2:c.796+32C>T XP_006720089.1:n.796+32C>T
XM_011536412.1:c.925+32C>T XP_011534714.1:n.925+32C>T
XM_011536413.1:c.610+32C>T XP_011534715.1:n.610+32C>T
XM_011536414.1:c.607+32C>T XP_011534716.1:n.607+32C>T
XM_011536415.1:c.178+32C>T XP_011534717.1:n.178+32C>T
NM_001320424.1:c.178+32C>T NP_001307353.1:n.178+32C>T
NM_152328.4:c.793+32C>T NP_689541.1:n.793+32C>T
NM_199165.2:c.922+32C>T NP_954634.1:n.922+32C>T
XM_006720026.3:c.796+32C>T XP_006720089.1:n.796+32C>T
XM_011536412.2:c.925+32C>T XP_011534714.1:n.925+32C>T
XR_001750917.1:n.434G>A
NM_152328.5:c.793+32C>T MANE Select NP_689541.1:n.793+32C>T