Canonical Allele Identifier: CA375230672

Gene: ASS1

Linked Data

• gnomAD v4: 9-130489420-T-C
• MyVariant Identifiers: chr9:g.133364807T>C (hg19) ; chr9:g.130489420T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489420T>C , CM000671.2:g.130489420T>C	GRCh38
NC_000009.11:g.133364807T>C , CM000671.1:g.133364807T>C	GRCh37
NC_000009.10:g.132354628T>C	NCBI36
NG_011542.1:g.49714T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.926T>C MANE Select	ENSP00000253004.6:p.Ile309Thr
ENST00000352480.9:c.926T>C	ENSP00000253004.6:p.Ile309Thr
ENST00000372386.6:n.197T>C
ENST00000372393.7:c.926T>C	ENSP00000361469.2:p.Ile309Thr
ENST00000372394.5:c.926T>C	ENSP00000361471.1:p.Ile309Thr
ENST00000470849.4:n.651T>C
ENST00000492400.5:n.435T>C
NM_000050.4:c.926T>C	NP_000041.2:p.Ile309Thr
NM_054012.3:c.926T>C	NP_446464.1:p.Ile309Thr
XM_005272200.2:c.926T>C	XP_005272257.1:p.Ile309Thr
XM_011518705.1:c.1040T>C	XP_011517007.1:p.Ile347Thr
XM_005272200.3:c.926T>C	XP_005272257.1:p.Ile309Thr
XM_011518705.2:c.1040T>C	XP_011517007.1:p.Ile347Thr
XM_017014729.1:c.1022T>C	XP_016870218.1:p.Ile341Thr
NM_054012.4:c.926T>C MANE Select	NP_446464.1:p.Ile309Thr