Canonical Allele Identifier: CA2261183014

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44008040A= , CM000679.2:g.44008040A=	GRCh38
NC_000017.10:g.42085408A= , CM000679.1:g.42085408A=	GRCh37
NC_000017.9:g.39440934A=	NCBI36
NG_008106.1:g.8377A=
NG_023338.1:g.1430T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+267A= (NAGS) MANE Select	ENSP00000293404.2:n.1451+267A=
ENST00000293404.7:c.1451+267A= (NAGS)	ENSP00000293404.2:n.1451+267A=
ENST00000589767.1:c.1382+267A= (NAGS)	ENSP00000465408.1:n.1382+267A=
ENST00000592915.1:n.1339+267A= (NAGS)
NM_153006.2:c.1451+267A= (NAGS)	NP_694551.1:n.1451+267A=
XM_011524438.1:c.1269-408A= (NAGS)	XP_011522740.1:n.1269-408A=
XM_011524439.1:c.953+267A= (NAGS)	XP_011522741.1:n.953+267A=
XM_011525035.1:c.-463+15532T= (PYY)	XP_011523337.1:n.-463+15532T=
XM_011524439.2:c.953+267A= (NAGS)	XP_011522741.1:n.953+267A=
NM_153006.3:c.1451+267A= (NAGS) MANE Select	NP_694551.1:n.1451+267A=