Canonical Allele Identifier: CA576362270

Gene: ASNS

Linked Data

• dbSNP Id: rs1443782997
• gnomAD v2: 7-97482561-A-C
• gnomAD v4: 7-97853249-A-C
• MyVariant Identifiers: chr7:g.97482561A>C (hg19) ; chr7:g.97853249A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97853249A>C , CM000669.2:g.97853249A>C	GRCh38
NC_000007.13:g.97482561A>C , CM000669.1:g.97482561A>C	GRCh37
NC_000007.12:g.97320497A>C	NCBI36
NG_033870.1:g.24294T>G
NG_033870.2:g.80314T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394308.8:c.1321-34T>G MANE Select	ENSP00000377845.3:n.1321-34T>G
ENST00000175506.8:c.1321-34T>G	ENSP00000175506.4:n.1321-34T>G
ENST00000394308.7:c.1321-34T>G	ENSP00000377845.3:n.1321-34T>G
ENST00000394309.7:c.1321-34T>G	ENSP00000377846.3:n.1321-34T>G
ENST00000422745.5:c.1258-34T>G	ENSP00000414901.1:n.1258-34T>G
ENST00000437628.5:c.1072-34T>G	ENSP00000414379.1:n.1072-34T>G
ENST00000444334.5:c.1258-34T>G	ENSP00000406994.1:n.1258-34T>G
ENST00000454046.5:c.*189-34T>G	ENSP00000401651.1:n.*189-34T>G
ENST00000455086.5:c.1072-34T>G	ENSP00000408472.1:n.1072-34T>G
ENST00000487714.1:n.379-34T>G
NM_001178075.1:c.1258-34T>G	NP_001171546.1:n.1258-34T>G
NM_001178076.1:c.1072-34T>G	NP_001171547.1:n.1072-34T>G
NM_001178077.1:c.1072-34T>G	NP_001171548.1:n.1072-34T>G
NM_001673.4:c.1321-34T>G	NP_001664.3:n.1321-34T>G
NM_133436.3:c.1321-34T>G	NP_597680.2:n.1321-34T>G
NM_183356.3:c.1321-34T>G	NP_899199.2:n.1321-34T>G
NM_001352496.1:c.1321-34T>G	NP_001339425.1:n.1321-34T>G
NR_147989.1:n.3024-34T>G
NM_001673.5:c.1321-34T>G MANE Select	NP_001664.3:n.1321-34T>G
NM_001178075.2:c.1258-34T>G	NP_001171546.1:n.1258-34T>G
NM_001178076.2:c.1072-34T>G	NP_001171547.1:n.1072-34T>G
NM_001352496.2:c.1321-34T>G	NP_001339425.1:n.1321-34T>G
NM_183356.4:c.1321-34T>G	NP_899199.2:n.1321-34T>G