Canonical Allele Identifier: CA399725447

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42083460T>C (hg19) ; chr17:g.44006092T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006092T>C , CM000679.2:g.44006092T>C	GRCh38
NC_000017.10:g.42083460T>C , CM000679.1:g.42083460T>C	GRCh37
NC_000017.9:g.39438986T>C	NCBI36
NG_008106.1:g.6429T>C
NG_023338.1:g.3378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.770T>C (NAGS) MANE Select	ENSP00000293404.2:p.Ile257Thr
ENST00000293404.7:c.770T>C (NAGS)	ENSP00000293404.2:p.Ile257Thr
ENST00000589767.1:c.677T>C (NAGS)	ENSP00000465408.1:p.Ile226Thr
ENST00000592915.1:n.45T>C (NAGS)
NM_153006.2:c.770T>C (NAGS)	NP_694551.1:p.Ile257Thr
XM_011524438.1:c.770T>C (NAGS)	XP_011522740.1:p.Ile257Thr
XM_011524439.1:c.272T>C (NAGS)	XP_011522741.1:p.Ile91Thr
XM_011525035.1:c.-463+17480A>G (PYY)	XP_011523337.1:n.-463+17480A>G
XM_011524439.2:c.272T>C (NAGS)	XP_011522741.1:p.Ile91Thr
NM_153006.3:c.770T>C (NAGS) MANE Select	NP_694551.1:p.Ile257Thr