Canonical Allele Identifier: CA386304968

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101786104-G-A
• MyVariant Identifiers: chr12:g.102179882G>A (hg19) ; chr12:g.101786104G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786104G>A , CM000674.2:g.101786104G>A	GRCh38
NC_000012.11:g.102179882G>A , CM000674.1:g.102179882G>A	GRCh37
NC_000012.10:g.100704013G>A	NCBI36
NG_021243.1:g.49764C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.479C>T MANE Select	ENSP00000299314.7:p.Ser160Phe
ENST00000299314.11:c.479C>T	ENSP00000299314.7:p.Ser160Phe
ENST00000549940.5:c.479C>T	ENSP00000449150.1:p.Ser160Phe
ENST00000550352.1:n.273C>T
ENST00000552681.1:c.113C>T	ENSP00000449217.1:p.Ser38Phe
NM_024312.4:c.479C>T	NP_077288.2:p.Ser160Phe
XM_006719593.2:c.479C>T	XP_006719656.1:p.Ser160Phe
XM_011538731.1:c.398C>T	XP_011537033.1:p.Ser133Phe
XM_006719593.3:c.479C>T	XP_006719656.1:p.Ser160Phe
XM_011538731.2:c.398C>T	XP_011537033.1:p.Ser133Phe
XM_017019961.1:c.263C>T	XP_016875450.1:p.Ser88Phe
XM_017019962.2:c.-872C>T	XP_016875451.1:n.-872C>T
NM_024312.5:c.479C>T MANE Select	NP_077288.2:p.Ser160Phe