Canonical Allele Identifier: CA2261183007

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44008022C= , CM000679.2:g.44008022C=	GRCh38
NC_000017.10:g.42085390C= , CM000679.1:g.42085390C=	GRCh37
NC_000017.9:g.39440916C=	NCBI36
NG_008106.1:g.8359C=
NG_023338.1:g.1448G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+249C= (NAGS) MANE Select	ENSP00000293404.2:n.1451+249C=
ENST00000293404.7:c.1451+249C= (NAGS)	ENSP00000293404.2:n.1451+249C=
ENST00000589767.1:c.1382+249C= (NAGS)	ENSP00000465408.1:n.1382+249C=
ENST00000592915.1:n.1339+249C= (NAGS)
NM_153006.2:c.1451+249C= (NAGS)	NP_694551.1:n.1451+249C=
XM_011524438.1:c.1269-426C= (NAGS)	XP_011522740.1:n.1269-426C=
XM_011524439.1:c.953+249C= (NAGS)	XP_011522741.1:n.953+249C=
XM_011525035.1:c.-463+15550G= (PYY)	XP_011523337.1:n.-463+15550G=
XM_011524439.2:c.953+249C= (NAGS)	XP_011522741.1:n.953+249C=
NM_153006.3:c.1451+249C= (NAGS) MANE Select	NP_694551.1:n.1451+249C=