Canonical Allele Identifier: CA4354855

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97869140G>A , CM000669.2:g.97869140G>A	GRCh38
NC_000007.13:g.97498452G>A , CM000669.1:g.97498452G>A	GRCh37
NC_000007.12:g.97336388G>A	NCBI36
NG_033870.1:g.8403C>T
NG_033870.2:g.64423C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001673.5:c.17C>T MANE Select	NP_001664.3:p.Ala6Val
ENST00000394308.8:c.17C>T MANE Select	ENSP00000377845.3:p.Ala6Val
NM_001178075.1:c.-12-35C>T	NP_001171546.1:n.-12-35C>T
NM_001178075.2:c.-12-35C>T	NP_001171546.1:n.-12-35C>T
NM_001178076.1:c.-1+3211C>T	NP_001171547.1:n.-1+3211C>T
NM_001178076.2:c.-1+3211C>T	NP_001171547.1:n.-1+3211C>T
NM_001178077.1:c.-1+2901C>T	NP_001171548.1:n.-1+2901C>T
NM_001352496.1:c.17C>T	NP_001339425.1:p.Ala6Val
NM_001352496.2:c.17C>T	NP_001339425.1:p.Ala6Val
NM_001673.4:c.17C>T	NP_001664.3:p.Ala6Val
NM_133436.3:c.17C>T	NP_597680.2:p.Ala6Val
NM_183356.3:c.17C>T	NP_899199.2:p.Ala6Val
NM_183356.4:c.17C>T	NP_899199.2:p.Ala6Val
NR_147989.1:n.1646C>T
ENST00000175506.8:c.17C>T	ENSP00000175506.4:p.Ala6Val
ENST00000394308.7:c.17C>T	ENSP00000377845.3:p.Ala6Val
ENST00000394309.7:c.17C>T	ENSP00000377846.3:p.Ala6Val
ENST00000414884.1:c.17C>T	ENSP00000413797.1:p.Ala6Val
ENST00000422745.5:c.-12-35C>T	ENSP00000414901.1:n.-12-35C>T
ENST00000437628.5:c.-1+2901C>T	ENSP00000414379.1:n.-1+2901C>T
ENST00000437657.5:c.17C>T	ENSP00000394242.1:p.Ala6Val
ENST00000442734.5:c.17C>T	ENSP00000400422.1:p.Ala6Val
ENST00000444334.5:c.-12-35C>T	ENSP00000406994.1:n.-12-35C>T
ENST00000448127.1:c.17C>T	ENSP00000402350.1:p.Ala6Val
ENST00000451771.5:c.17C>T	ENSP00000397802.1:p.Ala6Val
ENST00000453600.5:c.-12-35C>T	ENSP00000408797.1:n.-12-35C>T
ENST00000454046.5:c.17C>T	ENSP00000401651.1:p.Ala6Val
ENST00000455086.5:c.-1+3211C>T	ENSP00000408472.1:n.-1+3211C>T
ENST00000495255.1:n.45C>T