Canonical Allele Identifier: CA1881244589

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452348_130452349delinsTG , CM000671.2:g.130452348_130452349delinsTG	GRCh38
NC_000009.11:g.133327735_133327736delinsTG , CM000671.1:g.133327735_133327736delinsTG	GRCh37
NC_000009.10:g.132317556_132317557delinsTG	NCBI36
NG_011542.1:g.12642_12643delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.105+15_105+16delinsTG MANE Select	ENSP00000253004.6:n.105+15_105+16delinsTG
ENST00000352480.9:c.105+15_105+16delinsTG	ENSP00000253004.6:n.105+15_105+16delinsTG
ENST00000372393.7:c.105+15_105+16delinsTG	ENSP00000361469.2:n.105+15_105+16delinsTG
ENST00000372394.5:c.105+15_105+16delinsTG	ENSP00000361471.1:n.105+15_105+16delinsTG
ENST00000422569.5:c.105+15_105+16delinsTG	ENSP00000394212.1:n.105+15_105+16delinsTG
ENST00000443588.1:c.105+15_105+16delinsTG	ENSP00000397785.1:n.105+15_105+16delinsTG
NM_000050.4:c.105+15_105+16delinsTG	NP_000041.2:n.105+15_105+16delinsTG
NM_054012.3:c.105+15_105+16delinsTG	NP_446464.1:n.105+15_105+16delinsTG
XM_005272200.2:c.105+15_105+16delinsTG	XP_005272257.1:n.105+15_105+16delinsTG
XM_011518705.1:c.219+15_219+16delinsTG	XP_011517007.1:n.219+15_219+16delinsTG
XM_005272200.3:c.105+15_105+16delinsTG	XP_005272257.1:n.105+15_105+16delinsTG
XM_011518705.2:c.219+15_219+16delinsTG	XP_011517007.1:n.219+15_219+16delinsTG
XM_017014729.1:c.201+15_201+16delinsTG	XP_016870218.1:n.201+15_201+16delinsTG
NM_054012.4:c.105+15_105+16delinsTG MANE Select	NP_446464.1:n.105+15_105+16delinsTG