Canonical Allele Identifier: CA15087751
Gene: ADSS2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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