Canonical Allele Identifier: CA2564536851

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489295_130489296insC , CM000671.2:g.130489295_130489296insC	GRCh38
NC_000009.11:g.133364682_133364683insC , CM000671.1:g.133364682_133364683insC	GRCh37
NC_000009.10:g.132354503_132354504insC	NCBI36
NG_011542.1:g.49589_49590insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-38_839-37insC MANE Select	ENSP00000253004.6:n.839-38_839-37insC
ENST00000352480.9:c.839-38_839-37insC	ENSP00000253004.6:n.839-38_839-37insC
ENST00000372386.6:n.110-38_110-37insC
ENST00000372393.7:c.839-38_839-37insC	ENSP00000361469.2:n.839-38_839-37insC
ENST00000372394.5:c.839-38_839-37insC	ENSP00000361471.1:n.839-38_839-37insC
ENST00000470849.4:n.564-38_564-37insC
ENST00000492400.5:n.348-38_348-37insC
ENST00000493984.6:n.616-38_616-37insC
NM_000050.4:c.839-38_839-37insC	NP_000041.2:n.839-38_839-37insC
NM_054012.3:c.839-38_839-37insC	NP_446464.1:n.839-38_839-37insC
XM_005272200.2:c.839-38_839-37insC	XP_005272257.1:n.839-38_839-37insC
XM_011518705.1:c.953-38_953-37insC	XP_011517007.1:n.953-38_953-37insC
XM_005272200.3:c.839-38_839-37insC	XP_005272257.1:n.839-38_839-37insC
XM_011518705.2:c.953-38_953-37insC	XP_011517007.1:n.953-38_953-37insC
XM_017014729.1:c.935-38_935-37insC	XP_016870218.1:n.935-38_935-37insC
NM_054012.4:c.839-38_839-37insC MANE Select	NP_446464.1:n.839-38_839-37insC