Canonical Allele Identifier: CA375230553

Gene: ASS1

Linked Data

• dbSNP Id: rs1257594301
• gnomAD v2: 9-133364771-T-C
• gnomAD v3: 9-130489384-T-C
• gnomAD v4: 9-130489384-T-C
• MyVariant Identifiers: chr9:g.133364771T>C (hg19) ; chr9:g.130489384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489384T>C , CM000671.2:g.130489384T>C	GRCh38
NC_000009.11:g.133364771T>C , CM000671.1:g.133364771T>C	GRCh37
NC_000009.10:g.132354592T>C	NCBI36
NG_011542.1:g.49678T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.890T>C MANE Select	ENSP00000253004.6:p.Ile297Thr
ENST00000352480.9:c.890T>C	ENSP00000253004.6:p.Ile297Thr
ENST00000372386.6:n.161T>C
ENST00000372393.7:c.890T>C	ENSP00000361469.2:p.Ile297Thr
ENST00000372394.5:c.890T>C	ENSP00000361471.1:p.Ile297Thr
ENST00000470849.4:n.615T>C
ENST00000492400.5:n.399T>C
ENST00000493984.6:n.667T>C
NM_000050.4:c.890T>C	NP_000041.2:p.Ile297Thr
NM_054012.3:c.890T>C	NP_446464.1:p.Ile297Thr
XM_005272200.2:c.890T>C	XP_005272257.1:p.Ile297Thr
XM_011518705.1:c.1004T>C	XP_011517007.1:p.Ile335Thr
XM_005272200.3:c.890T>C	XP_005272257.1:p.Ile297Thr
XM_011518705.2:c.1004T>C	XP_011517007.1:p.Ile335Thr
XM_017014729.1:c.986T>C	XP_016870218.1:p.Ile329Thr
NM_054012.4:c.890T>C MANE Select	NP_446464.1:p.Ile297Thr