Canonical Allele Identifier: CA1139986264
Gene: ADSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244413415C= , CM000663.2:g.244413415C= GRCh38
NC_000001.10:g.244576717C= , CM000663.1:g.244576717C= GRCh37
NC_000001.9:g.242643340C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366535.4:c.1169-1979G= MANE Select ENSP00000355493.3:n.1169-1979G=
ENST00000366535.3:c.1169-1979G= ENSP00000355493.3:n.1169-1979G=
ENST00000468215.1:n.738-1979G=
NM_001126.3:c.1169-1979G= NP_001117.2:n.1169-1979G=
XM_011544108.1:c.989-1979G= XP_011542410.1:n.989-1979G=
XM_011544109.1:c.989-1979G= XP_011542411.1:n.989-1979G=
NM_001126.4:c.1169-1979G= NP_001117.2:n.1169-1979G=
NM_001365073.1:c.1169-1988G= NP_001352002.1:n.1169-1988G=
XM_011544108.3:c.989-1979G= XP_011542410.1:n.989-1979G=
NM_001126.5:c.1169-1979G= MANE Select NP_001117.2:n.1169-1979G=
NM_001365073.2:c.1169-1988G= NP_001352002.1:n.1169-1988G=