Canonical Allele Identifier: CA1881244374

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452190_130452191delinsAG , CM000671.2:g.130452190_130452191delinsAG	GRCh38
NC_000009.11:g.133327577_133327578delinsAG , CM000671.1:g.133327577_133327578delinsAG	GRCh37
NC_000009.10:g.132317398_132317399delinsAG	NCBI36
NG_011542.1:g.12484_12485delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.-5-34_-5-33delinsAG MANE Select	ENSP00000253004.6:n.-5-34_-5-33delinsAG
ENST00000352480.9:c.-5-34_-5-33delinsAG	ENSP00000253004.6:n.-5-34_-5-33delinsAG
ENST00000372393.7:c.-5-34_-5-33delinsAG	ENSP00000361469.2:n.-5-34_-5-33delinsAG
ENST00000372394.5:c.-5-34_-5-33delinsAG	ENSP00000361471.1:n.-5-34_-5-33delinsAG
ENST00000422569.5:c.-5-34_-5-33delinsAG	ENSP00000394212.1:n.-5-34_-5-33delinsAG
NM_000050.4:c.-5-34_-5-33delinsAG	NP_000041.2:n.-5-34_-5-33delinsAG
NM_054012.3:c.-5-34_-5-33delinsAG	NP_446464.1:n.-5-34_-5-33delinsAG
XM_005272200.2:c.-5-34_-5-33delinsAG	XP_005272257.1:n.-5-34_-5-33delinsAG
XM_011518705.1:c.110-34_110-33delinsAG	XP_011517007.1:n.110-34_110-33delinsAG
XM_005272200.3:c.-5-34_-5-33delinsAG	XP_005272257.1:n.-5-34_-5-33delinsAG
XM_011518705.2:c.110-34_110-33delinsAG	XP_011517007.1:n.110-34_110-33delinsAG
XM_017014729.1:c.92-34_92-33delinsAG	XP_016870218.1:n.92-34_92-33delinsAG
NM_054012.4:c.-5-34_-5-33delinsAG MANE Select	NP_446464.1:n.-5-34_-5-33delinsAG