Canonical Allele Identifier: CA375226362

Gene: ASS1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130466723A>C , CM000671.2:g.130466723A>C	GRCh38
NC_000009.11:g.133342110A>C , CM000671.1:g.133342110A>C	GRCh37
NC_000009.10:g.132331931A>C	NCBI36
NG_011542.1:g.27017A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.421-2A>C MANE Select	ENSP00000253004.6:n.421-2A>C
ENST00000352480.9:c.421-2A>C	ENSP00000253004.6:n.421-2A>C
ENST00000372393.7:c.421-2A>C	ENSP00000361469.2:n.421-2A>C
ENST00000372394.5:c.421-2A>C	ENSP00000361471.1:n.421-2A>C
ENST00000422569.5:c.421-2A>C	ENSP00000394212.1:n.421-2A>C
ENST00000443588.1:c.364-2A>C	ENSP00000397785.1:n.364-2A>C
ENST00000467695.5:n.130-2A>C
ENST00000493984.6:n.250A>C
NM_000050.4:c.421-2A>C	NP_000041.2:n.421-2A>C
NM_054012.3:c.421-2A>C	NP_446464.1:n.421-2A>C
XM_005272200.2:c.421-2A>C	XP_005272257.1:n.421-2A>C
XM_011518705.1:c.535-2A>C	XP_011517007.1:n.535-2A>C
XM_005272200.3:c.421-2A>C	XP_005272257.1:n.421-2A>C
XM_011518705.2:c.535-2A>C	XP_011517007.1:n.535-2A>C
XM_017014729.1:c.517-2A>C	XP_016870218.1:n.517-2A>C
NM_054012.4:c.421-2A>C MANE Select	NP_446464.1:n.421-2A>C