Canonical Allele Identifier: CA1881271797

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480341_130480343delinsCCT , CM000671.2:g.130480341_130480343delinsCCT	GRCh38
NC_000009.11:g.133355728_133355730delinsCCT , CM000671.1:g.133355728_133355730delinsCCT	GRCh37
NC_000009.10:g.132345549_132345551delinsCCT	NCBI36
NG_011542.1:g.40635_40637delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.774-44_774-42delinsCCT MANE Select	ENSP00000253004.6:n.774-44_774-42delinsCC...
ENST00000352480.9:c.774-44_774-42delinsCCT	ENSP00000253004.6:n.774-44_774-42delinsCC...
ENST00000372386.6:n.45-44_45-42delinsCCT
ENST00000372393.7:c.774-44_774-42delinsCCT	ENSP00000361469.2:n.774-44_774-42delinsCC...
ENST00000372394.5:c.774-44_774-42delinsCCT	ENSP00000361471.1:n.774-44_774-42delinsCC...
ENST00000470849.4:n.499-44_499-42delinsCCT
ENST00000492400.5:n.283-44_283-42delinsCCT
ENST00000493984.6:n.551-44_551-42delinsCCT
NM_000050.4:c.774-44_774-42delinsCCT	NP_000041.2:n.774-44_774-42delinsCCT
NM_054012.3:c.774-44_774-42delinsCCT	NP_446464.1:n.774-44_774-42delinsCCT
XM_005272200.2:c.774-44_774-42delinsCCT	XP_005272257.1:n.774-44_774-42delinsCCT
XM_011518705.1:c.888-44_888-42delinsCCT	XP_011517007.1:n.888-44_888-42delinsCCT
XM_005272200.3:c.774-44_774-42delinsCCT	XP_005272257.1:n.774-44_774-42delinsCCT
XM_011518705.2:c.888-44_888-42delinsCCT	XP_011517007.1:n.888-44_888-42delinsCCT
XM_017014729.1:c.870-44_870-42delinsCCT	XP_016870218.1:n.870-44_870-42delinsCCT
NM_054012.4:c.774-44_774-42delinsCCT MANE Select	NP_446464.1:n.774-44_774-42delinsCCT