Canonical Allele Identifier: CA1881276633

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489385_130489386delinsCG , CM000671.2:g.130489385_130489386delinsCG	GRCh38
NC_000009.11:g.133364772_133364773delinsCG , CM000671.1:g.133364772_133364773delinsCG	GRCh37
NC_000009.10:g.132354593_132354594delinsCG	NCBI36
NG_011542.1:g.49679_49680delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.891_892delinsCG MANE Select	ENSP00000253004.6:p.Ile297=
ENST00000352480.9:c.891_892delinsCG	ENSP00000253004.6:p.Ile297=
ENST00000372386.6:n.162_163delinsCG
ENST00000372393.7:c.891_892delinsCG	ENSP00000361469.2:p.Ile297=
ENST00000372394.5:c.891_892delinsCG	ENSP00000361471.1:p.Ile297=
ENST00000470849.4:n.616_617delinsCG
ENST00000492400.5:n.400_401delinsCG
ENST00000493984.6:n.668_669delinsCG
NM_000050.4:c.891_892delinsCG	NP_000041.2:p.Ile297=
NM_054012.3:c.891_892delinsCG	NP_446464.1:p.Ile297=
XM_005272200.2:c.891_892delinsCG	XP_005272257.1:p.Ile297=
XM_011518705.1:c.1005_1006delinsCG	XP_011517007.1:p.Ile335=
XM_005272200.3:c.891_892delinsCG	XP_005272257.1:p.Ile297=
XM_011518705.2:c.1005_1006delinsCG	XP_011517007.1:p.Ile335=
XM_017014729.1:c.987_988delinsCG	XP_016870218.1:p.Ile329=
NM_054012.4:c.891_892delinsCG MANE Select	NP_446464.1:p.Ile297=