Canonical Allele Identifier: CA399727833

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42085064G>C (hg19) ; chr17:g.44007696G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007696G>C , CM000679.2:g.44007696G>C	GRCh38
NC_000017.10:g.42085064G>C , CM000679.1:g.42085064G>C	GRCh37
NC_000017.9:g.39440590G>C	NCBI36
NG_008106.1:g.8033G>C
NG_023338.1:g.1774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1374G>C (NAGS) MANE Select	ENSP00000293404.2:p.Gln458His
ENST00000293404.7:c.1374G>C (NAGS)	ENSP00000293404.2:p.Gln458His
ENST00000589767.1:c.1305G>C (NAGS)	ENSP00000465408.1:p.Gln435His
ENST00000592915.1:n.1262G>C (NAGS)
NM_153006.2:c.1374G>C (NAGS)	NP_694551.1:p.Gln458His
XM_011524438.1:c.1268+202G>C (NAGS)	XP_011522740.1:n.1268+202G>C
XM_011524439.1:c.876G>C (NAGS)	XP_011522741.1:p.Gln292His
XM_011525035.1:c.-463+15876C>G (PYY)	XP_011523337.1:n.-463+15876C>G
XM_011524439.2:c.876G>C (NAGS)	XP_011522741.1:p.Gln292His
NM_153006.3:c.1374G>C (NAGS) MANE Select	NP_694551.1:p.Gln458His