Canonical Allele Identifier: CA1881276591

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489277_130489278delinsGT , CM000671.2:g.130489277_130489278delinsGT	GRCh38
NC_000009.11:g.133364664_133364665delinsGT , CM000671.1:g.133364664_133364665delinsGT	GRCh37
NC_000009.10:g.132354485_132354486delinsGT	NCBI36
NG_011542.1:g.49571_49572delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-56_839-55delinsGT MANE Select	ENSP00000253004.6:n.839-56_839-55delinsGT
ENST00000352480.9:c.839-56_839-55delinsGT	ENSP00000253004.6:n.839-56_839-55delinsGT
ENST00000372386.6:n.110-56_110-55delinsGT
ENST00000372393.7:c.839-56_839-55delinsGT	ENSP00000361469.2:n.839-56_839-55delinsGT
ENST00000372394.5:c.839-56_839-55delinsGT	ENSP00000361471.1:n.839-56_839-55delinsGT
ENST00000470849.4:n.564-56_564-55delinsGT
ENST00000492400.5:n.348-56_348-55delinsGT
ENST00000493984.6:n.616-56_616-55delinsGT
NM_000050.4:c.839-56_839-55delinsGT	NP_000041.2:n.839-56_839-55delinsGT
NM_054012.3:c.839-56_839-55delinsGT	NP_446464.1:n.839-56_839-55delinsGT
XM_005272200.2:c.839-56_839-55delinsGT	XP_005272257.1:n.839-56_839-55delinsGT
XM_011518705.1:c.953-56_953-55delinsGT	XP_011517007.1:n.953-56_953-55delinsGT
XM_005272200.3:c.839-56_839-55delinsGT	XP_005272257.1:n.839-56_839-55delinsGT
XM_011518705.2:c.953-56_953-55delinsGT	XP_011517007.1:n.953-56_953-55delinsGT
XM_017014729.1:c.935-56_935-55delinsGT	XP_016870218.1:n.935-56_935-55delinsGT
NM_054012.4:c.839-56_839-55delinsGT MANE Select	NP_446464.1:n.839-56_839-55delinsGT