Canonical Allele Identifier: CA4354526

Gene: ASNS

Linked Data

• dbSNP Id: rs766974447
• ExAC: 7:97482568 A / G
• gnomAD v2: 7-97482568-A-G
• gnomAD v4: 7-97853256-A-G
• MyVariant Identifiers: chr7:g.97482568A>G (hg19) ; chr7:g.97853256A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97853256A>G , CM000669.2:g.97853256A>G	GRCh38
NC_000007.13:g.97482568A>G , CM000669.1:g.97482568A>G	GRCh37
NC_000007.12:g.97320504A>G	NCBI36
NG_033870.1:g.24287T>C
NG_033870.2:g.80307T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394308.8:c.1321-41T>C MANE Select	ENSP00000377845.3:n.1321-41T>C
ENST00000175506.8:c.1321-41T>C	ENSP00000175506.4:n.1321-41T>C
ENST00000394308.7:c.1321-41T>C	ENSP00000377845.3:n.1321-41T>C
ENST00000394309.7:c.1321-41T>C	ENSP00000377846.3:n.1321-41T>C
ENST00000422745.5:c.1258-41T>C	ENSP00000414901.1:n.1258-41T>C
ENST00000437628.5:c.1072-41T>C	ENSP00000414379.1:n.1072-41T>C
ENST00000444334.5:c.1258-41T>C	ENSP00000406994.1:n.1258-41T>C
ENST00000454046.5:c.*189-41T>C	ENSP00000401651.1:n.*189-41T>C
ENST00000455086.5:c.1072-41T>C	ENSP00000408472.1:n.1072-41T>C
ENST00000487714.1:n.379-41T>C
NM_001178075.1:c.1258-41T>C	NP_001171546.1:n.1258-41T>C
NM_001178076.1:c.1072-41T>C	NP_001171547.1:n.1072-41T>C
NM_001178077.1:c.1072-41T>C	NP_001171548.1:n.1072-41T>C
NM_001673.4:c.1321-41T>C	NP_001664.3:n.1321-41T>C
NM_133436.3:c.1321-41T>C	NP_597680.2:n.1321-41T>C
NM_183356.3:c.1321-41T>C	NP_899199.2:n.1321-41T>C
NM_001352496.1:c.1321-41T>C	NP_001339425.1:n.1321-41T>C
NR_147989.1:n.3024-41T>C
NM_001673.5:c.1321-41T>C MANE Select	NP_001664.3:n.1321-41T>C
NM_001178075.2:c.1258-41T>C	NP_001171546.1:n.1258-41T>C
NM_001178076.2:c.1072-41T>C	NP_001171547.1:n.1072-41T>C
NM_001352496.2:c.1321-41T>C	NP_001339425.1:n.1321-41T>C
NM_183356.4:c.1321-41T>C	NP_899199.2:n.1321-41T>C