Canonical Allele Identifier: CA2516250022

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489320G>T , CM000671.2:g.130489320G>T	GRCh38
NC_000009.11:g.133364707G>T , CM000671.1:g.133364707G>T	GRCh37
NC_000009.10:g.132354528G>T	NCBI36
NG_011542.1:g.49614G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-13G>T MANE Select	ENSP00000253004.6:n.839-13G>T
ENST00000352480.9:c.839-13G>T	ENSP00000253004.6:n.839-13G>T
ENST00000372386.6:n.110-13G>T
ENST00000372393.7:c.839-13G>T	ENSP00000361469.2:n.839-13G>T
ENST00000372394.5:c.839-13G>T	ENSP00000361471.1:n.839-13G>T
ENST00000470849.4:n.564-13G>T
ENST00000492400.5:n.348-13G>T
ENST00000493984.6:n.616-13G>T
NM_000050.4:c.839-13G>T	NP_000041.2:n.839-13G>T
NM_054012.3:c.839-13G>T	NP_446464.1:n.839-13G>T
XM_005272200.2:c.839-13G>T	XP_005272257.1:n.839-13G>T
XM_011518705.1:c.953-13G>T	XP_011517007.1:n.953-13G>T
XM_005272200.3:c.839-13G>T	XP_005272257.1:n.839-13G>T
XM_011518705.2:c.953-13G>T	XP_011517007.1:n.953-13G>T
XM_017014729.1:c.935-13G>T	XP_016870218.1:n.935-13G>T
NM_054012.4:c.839-13G>T MANE Select	NP_446464.1:n.839-13G>T