Canonical Allele Identifier: CA1881271813

Gene: ASS1

Linked Data

• dbSNP Id: rs1846137469

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480344_130480345insAG , CM000671.2:g.130480344_130480345insAG	GRCh38
NC_000009.11:g.133355731_133355732insAG , CM000671.1:g.133355731_133355732insAG	GRCh37
NC_000009.10:g.132345552_132345553insAG	NCBI36
NG_011542.1:g.40638_40639insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.774-41_774-40insAG MANE Select	ENSP00000253004.6:n.774-41_774-40insAG
ENST00000352480.9:c.774-41_774-40insAG	ENSP00000253004.6:n.774-41_774-40insAG
ENST00000372386.6:n.45-41_45-40insAG
ENST00000372393.7:c.774-41_774-40insAG	ENSP00000361469.2:n.774-41_774-40insAG
ENST00000372394.5:c.774-41_774-40insAG	ENSP00000361471.1:n.774-41_774-40insAG
ENST00000470849.4:n.499-41_499-40insAG
ENST00000492400.5:n.283-41_283-40insAG
ENST00000493984.6:n.551-41_551-40insAG
NM_000050.4:c.774-41_774-40insAG	NP_000041.2:n.774-41_774-40insAG
NM_054012.3:c.774-41_774-40insAG	NP_446464.1:n.774-41_774-40insAG
XM_005272200.2:c.774-41_774-40insAG	XP_005272257.1:n.774-41_774-40insAG
XM_011518705.1:c.888-41_888-40insAG	XP_011517007.1:n.888-41_888-40insAG
XM_005272200.3:c.774-41_774-40insAG	XP_005272257.1:n.774-41_774-40insAG
XM_011518705.2:c.888-41_888-40insAG	XP_011517007.1:n.888-41_888-40insAG
XM_017014729.1:c.870-41_870-40insAG	XP_016870218.1:n.870-41_870-40insAG
NM_054012.4:c.774-41_774-40insAG MANE Select	NP_446464.1:n.774-41_774-40insAG