Canonical Allele Identifier: CA1881276550

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489194_130489195delinsTG , CM000671.2:g.130489194_130489195delinsTG	GRCh38
NC_000009.11:g.133364581_133364582delinsTG , CM000671.1:g.133364581_133364582delinsTG	GRCh37
NC_000009.10:g.132354402_132354403delinsTG	NCBI36
NG_011542.1:g.49488_49489delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-139_839-138delinsTG MANE Select	ENSP00000253004.6:n.839-139_839-138delinsTG
ENST00000352480.9:c.839-139_839-138delinsTG	ENSP00000253004.6:n.839-139_839-138delinsTG
ENST00000372386.6:n.110-139_110-138delinsTG
ENST00000372393.7:c.839-139_839-138delinsTG	ENSP00000361469.2:n.839-139_839-138delinsTG
ENST00000372394.5:c.839-139_839-138delinsTG	ENSP00000361471.1:n.839-139_839-138delinsTG
ENST00000470849.4:n.564-139_564-138delinsTG
ENST00000492400.5:n.348-139_348-138delinsTG
ENST00000493984.6:n.616-139_616-138delinsTG
NM_000050.4:c.839-139_839-138delinsTG	NP_000041.2:n.839-139_839-138delinsTG
NM_054012.3:c.839-139_839-138delinsTG	NP_446464.1:n.839-139_839-138delinsTG
XM_005272200.2:c.839-139_839-138delinsTG	XP_005272257.1:n.839-139_839-138delinsTG
XM_011518705.1:c.953-139_953-138delinsTG	XP_011517007.1:n.953-139_953-138delinsTG
XM_005272200.3:c.839-139_839-138delinsTG	XP_005272257.1:n.839-139_839-138delinsTG
XM_011518705.2:c.953-139_953-138delinsTG	XP_011517007.1:n.953-139_953-138delinsTG
XM_017014729.1:c.935-139_935-138delinsTG	XP_016870218.1:n.935-139_935-138delinsTG
NM_054012.4:c.839-139_839-138delinsTG MANE Select	NP_446464.1:n.839-139_839-138delinsTG