Canonical Allele Identifier: CA2580079836

Gene: ASS1

Linked Data

• ClinVar Variation Id: 1944931
• ClinVar RCV Id: RCV002680685

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480468C>T , CM000671.2:g.130480468C>T	GRCh38
NC_000009.11:g.133355855C>T , CM000671.1:g.133355855C>T	GRCh37
NC_000009.10:g.132345676C>T	NCBI36
NG_011542.1:g.40762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.838+19C>T MANE Select	ENSP00000253004.6:n.838+19C>T
ENST00000352480.9:c.838+19C>T	ENSP00000253004.6:n.838+19C>T
ENST00000372386.6:n.109+19C>T
ENST00000372393.7:c.838+19C>T	ENSP00000361469.2:n.838+19C>T
ENST00000372394.5:c.838+19C>T	ENSP00000361471.1:n.838+19C>T
ENST00000470849.4:n.563+19C>T
ENST00000492400.5:n.347+19C>T
ENST00000493984.6:n.615+19C>T
NM_000050.4:c.838+19C>T	NP_000041.2:n.838+19C>T
NM_054012.3:c.838+19C>T	NP_446464.1:n.838+19C>T
XM_005272200.2:c.838+19C>T	XP_005272257.1:n.838+19C>T
XM_011518705.1:c.952+19C>T	XP_011517007.1:n.952+19C>T
XM_005272200.3:c.838+19C>T	XP_005272257.1:n.838+19C>T
XM_011518705.2:c.952+19C>T	XP_011517007.1:n.952+19C>T
XM_017014729.1:c.934+19C>T	XP_016870218.1:n.934+19C>T
NM_054012.4:c.838+19C>T MANE Select	NP_446464.1:n.838+19C>T