Canonical Allele Identifier: CA375230734

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133364821G>T (hg19) ; chr9:g.130489434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489434G>T , CM000671.2:g.130489434G>T	GRCh38
NC_000009.11:g.133364821G>T , CM000671.1:g.133364821G>T	GRCh37
NC_000009.10:g.132354642G>T	NCBI36
NG_011542.1:g.49728G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.940G>T MANE Select	ENSP00000253004.6:p.Gly314Cys
ENST00000352480.9:c.940G>T	ENSP00000253004.6:p.Gly314Cys
ENST00000372386.6:n.211G>T
ENST00000372393.7:c.940G>T	ENSP00000361469.2:p.Gly314Cys
ENST00000372394.5:c.940G>T	ENSP00000361471.1:p.Gly314Cys
NM_000050.4:c.940G>T	NP_000041.2:p.Gly314Cys
NM_054012.3:c.940G>T	NP_446464.1:p.Gly314Cys
XM_005272200.2:c.940G>T	XP_005272257.1:p.Gly314Cys
XM_011518705.1:c.1054G>T	XP_011517007.1:p.Gly352Cys
XM_005272200.3:c.940G>T	XP_005272257.1:p.Gly314Cys
XM_011518705.2:c.1054G>T	XP_011517007.1:p.Gly352Cys
XM_017014729.1:c.1036G>T	XP_016870218.1:p.Gly346Cys
NM_054012.4:c.940G>T MANE Select	NP_446464.1:p.Gly314Cys