Canonical Allele Identifier: CA399725436

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44006086-T-G
• MyVariant Identifiers: chr17:g.42083454T>G (hg19) ; chr17:g.44006086T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006086T>G , CM000679.2:g.44006086T>G	GRCh38
NC_000017.10:g.42083454T>G , CM000679.1:g.42083454T>G	GRCh37
NC_000017.9:g.39438980T>G	NCBI36
NG_008106.1:g.6423T>G
NG_023338.1:g.3384A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.764T>G (NAGS) MANE Select	ENSP00000293404.2:p.Ile255Ser
ENST00000293404.7:c.764T>G (NAGS)	ENSP00000293404.2:p.Ile255Ser
ENST00000589767.1:c.671T>G (NAGS)	ENSP00000465408.1:p.Ile224Ser
ENST00000592915.1:n.39T>G (NAGS)
NM_153006.2:c.764T>G (NAGS)	NP_694551.1:p.Ile255Ser
XM_011524438.1:c.764T>G (NAGS)	XP_011522740.1:p.Ile255Ser
XM_011524439.1:c.266T>G (NAGS)	XP_011522741.1:p.Ile89Ser
XM_011525035.1:c.-463+17486A>C (PYY)	XP_011523337.1:n.-463+17486A>C
XM_011524439.2:c.266T>G (NAGS)	XP_011522741.1:p.Ile89Ser
NM_153006.3:c.764T>G (NAGS) MANE Select	NP_694551.1:p.Ile255Ser