Canonical Allele Identifier: CA375232709

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133374937C>G (hg19) ; chr9:g.130499550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130499550C>G , CM000671.2:g.130499550C>G	GRCh38
NC_000009.11:g.133374937C>G , CM000671.1:g.133374937C>G	GRCh37
NC_000009.10:g.132364758C>G	NCBI36
NG_011542.1:g.59844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.1173C>G MANE Select	ENSP00000253004.6:p.Phe391Leu
ENST00000352480.9:c.1173C>G	ENSP00000253004.6:p.Phe391Leu
ENST00000372386.6:n.444C>G
ENST00000372393.7:c.1173C>G	ENSP00000361469.2:p.Phe391Leu
ENST00000372394.5:c.1173C>G	ENSP00000361471.1:p.Phe391Leu
NM_000050.4:c.1173C>G	NP_000041.2:p.Phe391Leu
NM_054012.3:c.1173C>G	NP_446464.1:p.Phe391Leu
XM_005272200.2:c.1173C>G	XP_005272257.1:p.Phe391Leu
XM_011518705.1:c.1287C>G	XP_011517007.1:p.Phe429Leu
XR_930393.1:n.1059+397G>C
XM_005272200.3:c.1173C>G	XP_005272257.1:p.Phe391Leu
XM_011518705.2:c.1287C>G	XP_011517007.1:p.Phe429Leu
XM_017014729.1:c.1269C>G	XP_016870218.1:p.Phe423Leu
XR_930393.2:n.1101+397G>C
NM_054012.4:c.1173C>G MANE Select	NP_446464.1:p.Phe391Leu