Canonical Allele Identifier: CA2580077927

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97858410A>C , CM000669.2:g.97858410A>C	GRCh38
NC_000007.13:g.97487722A>C , CM000669.1:g.97487722A>C	GRCh37
NC_000007.12:g.97325658A>C	NCBI36
NG_033870.1:g.19133T>G
NG_033870.2:g.75153T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394308.8:c.776-5T>G MANE Select	ENSP00000377845.3:n.776-5T>G
ENST00000175506.8:c.776-5T>G	ENSP00000175506.4:n.776-5T>G
ENST00000394308.7:c.776-5T>G	ENSP00000377845.3:n.776-5T>G
ENST00000394309.7:c.776-5T>G	ENSP00000377846.3:n.776-5T>G
ENST00000422745.5:c.713-5T>G	ENSP00000414901.1:n.713-5T>G
ENST00000437628.5:c.527-5T>G	ENSP00000414379.1:n.527-5T>G
ENST00000444334.5:c.713-5T>G	ENSP00000406994.1:n.713-5T>G
ENST00000454046.5:c.776-5T>G	ENSP00000401651.1:n.776-5T>G
ENST00000455086.5:c.527-5T>G	ENSP00000408472.1:n.527-5T>G
NM_001178075.1:c.713-5T>G	NP_001171546.1:n.713-5T>G
NM_001178076.1:c.527-5T>G	NP_001171547.1:n.527-5T>G
NM_001178077.1:c.527-5T>G	NP_001171548.1:n.527-5T>G
NM_001673.4:c.776-5T>G	NP_001664.3:n.776-5T>G
NM_133436.3:c.776-5T>G	NP_597680.2:n.776-5T>G
NM_183356.3:c.776-5T>G	NP_899199.2:n.776-5T>G
NM_001352496.1:c.776-5T>G	NP_001339425.1:n.776-5T>G
NR_147989.1:n.2405-5T>G
NM_001673.5:c.776-5T>G MANE Select	NP_001664.3:n.776-5T>G
NM_001178075.2:c.713-5T>G	NP_001171546.1:n.713-5T>G
NM_001178076.2:c.527-5T>G	NP_001171547.1:n.527-5T>G
NM_001352496.2:c.776-5T>G	NP_001339425.1:n.776-5T>G
NM_183356.4:c.776-5T>G	NP_899199.2:n.776-5T>G