Canonical Allele Identifier: CA399726278

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42083982G>C (hg19) ; chr17:g.44006614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006614G>C , CM000679.2:g.44006614G>C	GRCh38
NC_000017.10:g.42083982G>C , CM000679.1:g.42083982G>C	GRCh37
NC_000017.9:g.39439508G>C	NCBI36
NG_008106.1:g.6951G>C
NG_023338.1:g.2856C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1001G>C (NAGS) MANE Select	ENSP00000293404.2:p.Arg334Pro
ENST00000293404.7:c.1001G>C (NAGS)	ENSP00000293404.2:p.Arg334Pro
ENST00000589767.1:c.908G>C (NAGS)	ENSP00000465408.1:p.Arg303Pro
ENST00000592915.1:n.276G>C (NAGS)
NM_153006.2:c.1001G>C (NAGS)	NP_694551.1:p.Arg334Pro
XM_011524438.1:c.1001G>C (NAGS)	XP_011522740.1:p.Arg334Pro
XM_011524439.1:c.503G>C (NAGS)	XP_011522741.1:p.Arg168Pro
XM_011525035.1:c.-463+16958C>G (PYY)	XP_011523337.1:n.-463+16958C>G
XM_011524439.2:c.503G>C (NAGS)	XP_011522741.1:p.Arg168Pro
NM_153006.3:c.1001G>C (NAGS) MANE Select	NP_694551.1:p.Arg334Pro