Canonical Allele Identifier: CA2692120188
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130471420_130471421dup , CM000671.2:g.130471420_130471421dup GRCh38
NC_000009.11:g.133346807_133346808dup , CM000671.1:g.133346807_133346808dup GRCh37
NC_000009.10:g.132336628_132336629dup NCBI36
NG_011542.1:g.31714_31715dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.567-65_567-64dup MANE Select ENSP00000253004.6:n.567-65_567-64dup
ENST00000352480.9:c.567-65_567-64dup ENSP00000253004.6:n.567-65_567-64dup
ENST00000372393.7:c.567-65_567-64dup ENSP00000361469.2:n.567-65_567-64dup
ENST00000372394.5:c.567-65_567-64dup ENSP00000361471.1:n.567-65_567-64dup
ENST00000422569.5:c.567-65_567-64dup ENSP00000394212.1:n.567-65_567-64dup
ENST00000443588.1:c.510-65_510-64dup ENSP00000397785.1:n.510-65_510-64dup
ENST00000467695.5:n.276-65_276-64dup
ENST00000493984.6:n.398-65_398-64dup
NM_000050.4:c.567-65_567-64dup NP_000041.2:n.567-65_567-64dup
NM_054012.3:c.567-65_567-64dup NP_446464.1:n.567-65_567-64dup
XM_005272200.2:c.567-65_567-64dup XP_005272257.1:n.567-65_567-64dup
XM_011518705.1:c.681-65_681-64dup XP_011517007.1:n.681-65_681-64dup
XM_005272200.3:c.567-65_567-64dup XP_005272257.1:n.567-65_567-64dup
XM_011518705.2:c.681-65_681-64dup XP_011517007.1:n.681-65_681-64dup
XM_017014729.1:c.663-65_663-64dup XP_016870218.1:n.663-65_663-64dup
NM_054012.4:c.567-65_567-64dup MANE Select NP_446464.1:n.567-65_567-64dup