Canonical Allele Identifier: CA368271071

Gene: ASNS

Linked Data

• MyVariant Identifiers: chr7:g.97493570C>G (hg19) ; chr7:g.97864258C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97864258C>G , CM000669.2:g.97864258C>G	GRCh38
NC_000007.13:g.97493570C>G , CM000669.1:g.97493570C>G	GRCh37
NC_000007.12:g.97331506C>G	NCBI36
NG_033870.1:g.13285G>C
NG_033870.2:g.69305G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394308.8:c.487+1G>C MANE Select	ENSP00000377845.3:n.487+1G>C
ENST00000175506.8:c.487+1G>C	ENSP00000175506.4:n.487+1G>C
ENST00000394308.7:c.487+1G>C	ENSP00000377845.3:n.487+1G>C
ENST00000394309.7:c.487+1G>C	ENSP00000377846.3:n.487+1G>C
ENST00000422745.5:c.424+1G>C	ENSP00000414901.1:n.424+1G>C
ENST00000437628.5:c.238+1G>C	ENSP00000414379.1:n.238+1G>C
ENST00000442734.5:c.487+1G>C	ENSP00000400422.1:n.487+1G>C
ENST00000444334.5:c.424+1G>C	ENSP00000406994.1:n.424+1G>C
ENST00000454046.5:c.487+1G>C	ENSP00000401651.1:n.487+1G>C
ENST00000455086.5:c.238+1G>C	ENSP00000408472.1:n.238+1G>C
ENST00000495255.1:n.516G>C
NM_001178075.1:c.424+1G>C	NP_001171546.1:n.424+1G>C
NM_001178076.1:c.238+1G>C	NP_001171547.1:n.238+1G>C
NM_001178077.1:c.238+1G>C	NP_001171548.1:n.238+1G>C
NM_001673.4:c.487+1G>C	NP_001664.3:n.487+1G>C
NM_133436.3:c.487+1G>C	NP_597680.2:n.487+1G>C
NM_183356.3:c.487+1G>C	NP_899199.2:n.487+1G>C
NM_001352496.1:c.487+1G>C	NP_001339425.1:n.487+1G>C
NR_147989.1:n.2116+1G>C
NM_001673.5:c.487+1G>C MANE Select	NP_001664.3:n.487+1G>C
NM_001178075.2:c.424+1G>C	NP_001171546.1:n.424+1G>C
NM_001178076.2:c.238+1G>C	NP_001171547.1:n.238+1G>C
NM_001352496.2:c.487+1G>C	NP_001339425.1:n.487+1G>C
NM_183356.4:c.487+1G>C	NP_899199.2:n.487+1G>C