Canonical Allele Identifier: CA2832555786

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130452175_130452176dup , CM000671.2:g.130452175_130452176dup	GRCh38
NC_000009.11:g.133327562_133327563dup , CM000671.1:g.133327562_133327563dup	GRCh37
NC_000009.10:g.132317383_132317384dup	NCBI36
NG_011542.1:g.12469_12470dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.-5-49_-5-48dup MANE Select	ENSP00000253004.6:n.-5-49_-5-48dup
ENST00000352480.9:c.-5-49_-5-48dup	ENSP00000253004.6:n.-5-49_-5-48dup
ENST00000372393.7:c.-5-49_-5-48dup	ENSP00000361469.2:n.-5-49_-5-48dup
ENST00000372394.5:c.-5-49_-5-48dup	ENSP00000361471.1:n.-5-49_-5-48dup
ENST00000422569.5:c.-5-49_-5-48dup	ENSP00000394212.1:n.-5-49_-5-48dup
NM_000050.4:c.-5-49_-5-48dup	NP_000041.2:n.-5-49_-5-48dup
NM_054012.3:c.-5-49_-5-48dup	NP_446464.1:n.-5-49_-5-48dup
XM_005272200.2:c.-5-49_-5-48dup	XP_005272257.1:n.-5-49_-5-48dup
XM_011518705.1:c.110-49_110-48dup	XP_011517007.1:n.110-49_110-48dup
XM_005272200.3:c.-5-49_-5-48dup	XP_005272257.1:n.-5-49_-5-48dup
XM_011518705.2:c.110-49_110-48dup	XP_011517007.1:n.110-49_110-48dup
XM_017014729.1:c.92-49_92-48dup	XP_016870218.1:n.92-49_92-48dup
NM_054012.4:c.-5-49_-5-48dup MANE Select	NP_446464.1:n.-5-49_-5-48dup