Canonical Allele Identifier: CA399726521

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42084056A>G (hg19) ; chr17:g.44006688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006688A>G , CM000679.2:g.44006688A>G	GRCh38
NC_000017.10:g.42084056A>G , CM000679.1:g.42084056A>G	GRCh37
NC_000017.9:g.39439582A>G	NCBI36
NG_008106.1:g.7025A>G
NG_023338.1:g.2782T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1075A>G (NAGS) MANE Select	ENSP00000293404.2:p.Thr359Ala
ENST00000293404.7:c.1075A>G (NAGS)	ENSP00000293404.2:p.Thr359Ala
ENST00000589767.1:c.982A>G (NAGS)	ENSP00000465408.1:p.Thr328Ala
ENST00000592915.1:n.350A>G (NAGS)
NM_153006.2:c.1075A>G (NAGS)	NP_694551.1:p.Thr359Ala
XM_011524438.1:c.1075A>G (NAGS)	XP_011522740.1:p.Thr359Ala
XM_011524439.1:c.577A>G (NAGS)	XP_011522741.1:p.Thr193Ala
XM_011525035.1:c.-463+16884T>C (PYY)	XP_011523337.1:n.-463+16884T>C
XM_011524439.2:c.577A>G (NAGS)	XP_011522741.1:p.Thr193Ala
NM_153006.3:c.1075A>G (NAGS) MANE Select	NP_694551.1:p.Thr359Ala