Canonical Allele Identifier: CA1881271709
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130480195_130480197delinsTCA , CM000671.2:g.130480195_130480197delinsTCA GRCh38
NC_000009.11:g.133355582_133355584delinsTCA , CM000671.1:g.133355582_133355584delinsTCA GRCh37
NC_000009.10:g.132345403_132345405delinsTCA NCBI36
NG_011542.1:g.40489_40491delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.774-190_774-188delinsTCA MANE Select ENSP00000253004.6:n.774-190_774-188delinsTCA
ENST00000352480.9:c.774-190_774-188delinsTCA ENSP00000253004.6:n.774-190_774-188delinsTCA
ENST00000372386.6:n.45-190_45-188delinsTCA
ENST00000372393.7:c.774-190_774-188delinsTCA ENSP00000361469.2:n.774-190_774-188delinsTCA
ENST00000372394.5:c.774-190_774-188delinsTCA ENSP00000361471.1:n.774-190_774-188delinsTCA
ENST00000470849.4:n.499-190_499-188delinsTCA
ENST00000492400.5:n.283-190_283-188delinsTCA
ENST00000493984.6:n.551-190_551-188delinsTCA
NM_000050.4:c.774-190_774-188delinsTCA NP_000041.2:n.774-190_774-188delinsTCA
NM_054012.3:c.774-190_774-188delinsTCA NP_446464.1:n.774-190_774-188delinsTCA
XM_005272200.2:c.774-190_774-188delinsTCA XP_005272257.1:n.774-190_774-188delinsTCA
XM_011518705.1:c.888-190_888-188delinsTCA XP_011517007.1:n.888-190_888-188delinsTCA
XM_005272200.3:c.774-190_774-188delinsTCA XP_005272257.1:n.774-190_774-188delinsTCA
XM_011518705.2:c.888-190_888-188delinsTCA XP_011517007.1:n.888-190_888-188delinsTCA
XM_017014729.1:c.870-190_870-188delinsTCA XP_016870218.1:n.870-190_870-188delinsTCA
NM_054012.4:c.774-190_774-188delinsTCA MANE Select NP_446464.1:n.774-190_774-188delinsTCA