Canonical Allele Identifier: CA2520181559

Gene: ASS1

Linked Data

• gnomAD v4: 9-130489486-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489486C>T , CM000671.2:g.130489486C>T	GRCh38
NC_000009.11:g.133364873C>T , CM000671.1:g.133364873C>T	GRCh37
NC_000009.10:g.132354694C>T	NCBI36
NG_011542.1:g.49780C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.970+22C>T MANE Select	ENSP00000253004.6:n.970+22C>T
ENST00000352480.9:c.970+22C>T	ENSP00000253004.6:n.970+22C>T
ENST00000372386.6:n.241+22C>T
ENST00000372393.7:c.970+22C>T	ENSP00000361469.2:n.970+22C>T
ENST00000372394.5:c.970+22C>T	ENSP00000361471.1:n.970+22C>T
NM_000050.4:c.970+22C>T	NP_000041.2:n.970+22C>T
NM_054012.3:c.970+22C>T	NP_446464.1:n.970+22C>T
XM_005272200.2:c.970+22C>T	XP_005272257.1:n.970+22C>T
XM_011518705.1:c.1084+22C>T	XP_011517007.1:n.1084+22C>T
XM_005272200.3:c.970+22C>T	XP_005272257.1:n.970+22C>T
XM_011518705.2:c.1084+22C>T	XP_011517007.1:n.1084+22C>T
XM_017014729.1:c.1066+22C>T	XP_016870218.1:n.1066+22C>T
NM_054012.4:c.970+22C>T MANE Select	NP_446464.1:n.970+22C>T