Canonical Allele Identifier: CA368273885

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97868955G>T , CM000669.2:g.97868955G>T	GRCh38
NC_000007.13:g.97498267G>T , CM000669.1:g.97498267G>T	GRCh37
NC_000007.12:g.97336203G>T	NCBI36
NG_033870.1:g.8588C>A
NG_033870.2:g.64608C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394308.8:c.202C>A MANE Select	ENSP00000377845.3:p.Pro68Thr
ENST00000175506.8:c.202C>A	ENSP00000175506.4:p.Pro68Thr
ENST00000394308.7:c.202C>A	ENSP00000377845.3:p.Pro68Thr
ENST00000394309.7:c.202C>A	ENSP00000377846.3:p.Pro68Thr
ENST00000422745.5:c.139C>A	ENSP00000414901.1:p.Pro47Thr
ENST00000437628.5:c.-1+3086C>A	ENSP00000414379.1:n.-1+3086C>A
ENST00000437657.5:c.202C>A	ENSP00000394242.1:p.Pro68Thr
ENST00000442734.5:c.202C>A	ENSP00000400422.1:p.Pro68Thr
ENST00000444334.5:c.139C>A	ENSP00000406994.1:p.Pro47Thr
ENST00000448127.1:c.202C>A	ENSP00000402350.1:p.Pro68Thr
ENST00000453600.5:c.139C>A	ENSP00000408797.1:p.Pro47Thr
ENST00000454046.5:c.202C>A	ENSP00000401651.1:p.Pro68Thr
ENST00000455086.5:c.-1+3396C>A	ENSP00000408472.1:n.-1+3396C>A
ENST00000495255.1:n.230C>A
NM_001178075.1:c.139C>A	NP_001171546.1:p.Pro47Thr
NM_001178076.1:c.-1+3396C>A	NP_001171547.1:n.-1+3396C>A
NM_001178077.1:c.-1+3086C>A	NP_001171548.1:n.-1+3086C>A
NM_001673.4:c.202C>A	NP_001664.3:p.Pro68Thr
NM_133436.3:c.202C>A	NP_597680.2:p.Pro68Thr
NM_183356.3:c.202C>A	NP_899199.2:p.Pro68Thr
NM_001352496.1:c.202C>A	NP_001339425.1:p.Pro68Thr
NR_147989.1:n.1831C>A
NM_001673.5:c.202C>A MANE Select	NP_001664.3:p.Pro68Thr
NM_001178075.2:c.139C>A	NP_001171546.1:p.Pro47Thr
NM_001178076.2:c.-1+3396C>A	NP_001171547.1:n.-1+3396C>A
NM_001352496.2:c.202C>A	NP_001339425.1:p.Pro68Thr
NM_183356.4:c.202C>A	NP_899199.2:p.Pro68Thr