Canonical Allele Identifier: CA2638147005

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs2143991748
• gnomAD v4: 17-44007814-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007814T>C , CM000679.2:g.44007814T>C	GRCh38
NC_000017.10:g.42085182T>C , CM000679.1:g.42085182T>C	GRCh37
NC_000017.9:g.39440708T>C	NCBI36
NG_008106.1:g.8151T>C
NG_023338.1:g.1656A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+41T>C (NAGS) MANE Select	ENSP00000293404.2:n.1451+41T>C
ENST00000293404.7:c.1451+41T>C (NAGS)	ENSP00000293404.2:n.1451+41T>C
ENST00000589767.1:c.1382+41T>C (NAGS)	ENSP00000465408.1:n.1382+41T>C
ENST00000592915.1:n.1339+41T>C (NAGS)
NM_153006.2:c.1451+41T>C (NAGS)	NP_694551.1:n.1451+41T>C
XM_011524438.1:c.1268+320T>C (NAGS)	XP_011522740.1:n.1268+320T>C
XM_011524439.1:c.953+41T>C (NAGS)	XP_011522741.1:n.953+41T>C
XM_011525035.1:c.-463+15758A>G (PYY)	XP_011523337.1:n.-463+15758A>G
XM_011524439.2:c.953+41T>C (NAGS)	XP_011522741.1:n.953+41T>C
NM_153006.3:c.1451+41T>C (NAGS) MANE Select	NP_694551.1:n.1451+41T>C