Canonical Allele Identifier: CA1881271738

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480235_130480236delinsAC , CM000671.2:g.130480235_130480236delinsAC	GRCh38
NC_000009.11:g.133355622_133355623delinsAC , CM000671.1:g.133355622_133355623delinsAC	GRCh37
NC_000009.10:g.132345443_132345444delinsAC	NCBI36
NG_011542.1:g.40529_40530delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.774-150_774-149delinsAC MANE Select	ENSP00000253004.6:n.774-150_774-149delinsAC
ENST00000352480.9:c.774-150_774-149delinsAC	ENSP00000253004.6:n.774-150_774-149delinsAC
ENST00000372386.6:n.45-150_45-149delinsAC
ENST00000372393.7:c.774-150_774-149delinsAC	ENSP00000361469.2:n.774-150_774-149delinsAC
ENST00000372394.5:c.774-150_774-149delinsAC	ENSP00000361471.1:n.774-150_774-149delinsAC
ENST00000470849.4:n.499-150_499-149delinsAC
ENST00000492400.5:n.283-150_283-149delinsAC
ENST00000493984.6:n.551-150_551-149delinsAC
NM_000050.4:c.774-150_774-149delinsAC	NP_000041.2:n.774-150_774-149delinsAC
NM_054012.3:c.774-150_774-149delinsAC	NP_446464.1:n.774-150_774-149delinsAC
XM_005272200.2:c.774-150_774-149delinsAC	XP_005272257.1:n.774-150_774-149delinsAC
XM_011518705.1:c.888-150_888-149delinsAC	XP_011517007.1:n.888-150_888-149delinsAC
XM_005272200.3:c.774-150_774-149delinsAC	XP_005272257.1:n.774-150_774-149delinsAC
XM_011518705.2:c.888-150_888-149delinsAC	XP_011517007.1:n.888-150_888-149delinsAC
XM_017014729.1:c.870-150_870-149delinsAC	XP_016870218.1:n.870-150_870-149delinsAC
NM_054012.4:c.774-150_774-149delinsAC MANE Select	NP_446464.1:n.774-150_774-149delinsAC