Canonical Allele Identifier: CA375230576

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364782A>C (hg19) ; chr9:g.130489395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489395A>C , CM000671.2:g.130489395A>C	GRCh38
NC_000009.11:g.133364782A>C , CM000671.1:g.133364782A>C	GRCh37
NC_000009.10:g.132354603A>C	NCBI36
NG_011542.1:g.49689A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.901A>C MANE Select	ENSP00000253004.6:p.Thr301Pro
ENST00000352480.9:c.901A>C	ENSP00000253004.6:p.Thr301Pro
ENST00000372386.6:n.172A>C
ENST00000372393.7:c.901A>C	ENSP00000361469.2:p.Thr301Pro
ENST00000372394.5:c.901A>C	ENSP00000361471.1:p.Thr301Pro
ENST00000470849.4:n.626A>C
ENST00000492400.5:n.410A>C
ENST00000493984.6:n.678A>C
NM_000050.4:c.901A>C	NP_000041.2:p.Thr301Pro
NM_054012.3:c.901A>C	NP_446464.1:p.Thr301Pro
XM_005272200.2:c.901A>C	XP_005272257.1:p.Thr301Pro
XM_011518705.1:c.1015A>C	XP_011517007.1:p.Thr339Pro
XM_005272200.3:c.901A>C	XP_005272257.1:p.Thr301Pro
XM_011518705.2:c.1015A>C	XP_011517007.1:p.Thr339Pro
XM_017014729.1:c.997A>C	XP_016870218.1:p.Thr333Pro
NM_054012.4:c.901A>C MANE Select	NP_446464.1:p.Thr301Pro