Canonical Allele Identifier: CA386292271

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102147194T>A (hg19) ; chr12:g.101753416T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101753416T>A , CM000674.2:g.101753416T>A	GRCh38
NC_000012.11:g.102147194T>A , CM000674.1:g.102147194T>A	GRCh37
NC_000012.10:g.100671325T>A	NCBI36
NG_021243.1:g.82452A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.3558A>T MANE Select	ENSP00000299314.7:p.Arg1186Ser
ENST00000299314.11:c.3558A>T	ENSP00000299314.7:p.Arg1186Ser
ENST00000549738.5:c.456A>T	ENSP00000450161.1:n.456A>T
NM_024312.4:c.3558A>T	NP_077288.2:p.Arg1186Ser
XM_011538731.1:c.3477A>T	XP_011537033.1:p.Arg1159Ser
XM_011538731.2:c.3477A>T	XP_011537033.1:p.Arg1159Ser
XM_017019961.1:c.3342A>T	XP_016875450.1:p.Arg1114Ser
XM_017019962.2:c.2331A>T	XP_016875451.1:p.Arg777Ser
NM_024312.5:c.3558A>T MANE Select	NP_077288.2:p.Arg1186Ser