Canonical Allele Identifier: CA1881276594

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489288_130489290delinsTTC , CM000671.2:g.130489288_130489290delinsTTC	GRCh38
NC_000009.11:g.133364675_133364677delinsTTC , CM000671.1:g.133364675_133364677delinsTTC	GRCh37
NC_000009.10:g.132354496_132354498delinsTTC	NCBI36
NG_011542.1:g.49582_49584delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-45_839-43delinsTTC MANE Select	ENSP00000253004.6:n.839-45_839-43delinsTTC
ENST00000352480.9:c.839-45_839-43delinsTTC	ENSP00000253004.6:n.839-45_839-43delinsTTC
ENST00000372386.6:n.110-45_110-43delinsTTC
ENST00000372393.7:c.839-45_839-43delinsTTC	ENSP00000361469.2:n.839-45_839-43delinsTTC
ENST00000372394.5:c.839-45_839-43delinsTTC	ENSP00000361471.1:n.839-45_839-43delinsTTC
ENST00000470849.4:n.564-45_564-43delinsTTC
ENST00000492400.5:n.348-45_348-43delinsTTC
ENST00000493984.6:n.616-45_616-43delinsTTC
NM_000050.4:c.839-45_839-43delinsTTC	NP_000041.2:n.839-45_839-43delinsTTC
NM_054012.3:c.839-45_839-43delinsTTC	NP_446464.1:n.839-45_839-43delinsTTC
XM_005272200.2:c.839-45_839-43delinsTTC	XP_005272257.1:n.839-45_839-43delinsTTC
XM_011518705.1:c.953-45_953-43delinsTTC	XP_011517007.1:n.953-45_953-43delinsTTC
XM_005272200.3:c.839-45_839-43delinsTTC	XP_005272257.1:n.839-45_839-43delinsTTC
XM_011518705.2:c.953-45_953-43delinsTTC	XP_011517007.1:n.953-45_953-43delinsTTC
XM_017014729.1:c.935-45_935-43delinsTTC	XP_016870218.1:n.935-45_935-43delinsTTC
NM_054012.4:c.839-45_839-43delinsTTC MANE Select	NP_446464.1:n.839-45_839-43delinsTTC