Canonical Allele Identifier: CA626222656

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1419337957
• gnomAD v2: 17-42083637-C-A
• gnomAD v4: 17-44006269-C-A
• MyVariant Identifiers: chr17:g.42083637C>A (hg19) ; chr17:g.44006269C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006269C>A , CM000679.2:g.44006269C>A	GRCh38
NC_000017.10:g.42083637C>A , CM000679.1:g.42083637C>A	GRCh37
NC_000017.9:g.39439163C>A	NCBI36
NG_008106.1:g.6606C>A
NG_023338.1:g.3201G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.915+32C>A (NAGS) MANE Select	ENSP00000293404.2:n.915+32C>A
ENST00000293404.7:c.915+32C>A (NAGS)	ENSP00000293404.2:n.915+32C>A
ENST00000589767.1:c.822+32C>A (NAGS)	ENSP00000465408.1:n.822+32C>A
ENST00000592915.1:n.190+32C>A (NAGS)
NM_153006.2:c.915+32C>A (NAGS)	NP_694551.1:n.915+32C>A
XM_011524438.1:c.915+32C>A (NAGS)	XP_011522740.1:n.915+32C>A
XM_011524439.1:c.417+32C>A (NAGS)	XP_011522741.1:n.417+32C>A
XM_011525035.1:c.-463+17303G>T (PYY)	XP_011523337.1:n.-463+17303G>T
XM_011524439.2:c.417+32C>A (NAGS)	XP_011522741.1:n.417+32C>A
NM_153006.3:c.915+32C>A (NAGS) MANE Select	NP_694551.1:n.915+32C>A