Canonical Allele Identifier: CA386304853

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179831G>A (hg19) ; chr12:g.101786053G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786053G>A , CM000674.2:g.101786053G>A	GRCh38
NC_000012.11:g.102179831G>A , CM000674.1:g.102179831G>A	GRCh37
NC_000012.10:g.100703962G>A	NCBI36
NG_021243.1:g.49815C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.530C>T MANE Select	ENSP00000299314.7:p.Ser177Phe
ENST00000299314.11:c.530C>T	ENSP00000299314.7:p.Ser177Phe
ENST00000549940.5:c.530C>T	ENSP00000449150.1:p.Ser177Phe
ENST00000550352.1:n.324C>T
ENST00000552681.1:c.164C>T	ENSP00000449217.1:p.Ser55Phe
NM_024312.4:c.530C>T	NP_077288.2:p.Ser177Phe
XM_006719593.2:c.530C>T	XP_006719656.1:p.Ser177Phe
XM_011538731.1:c.449C>T	XP_011537033.1:p.Ser150Phe
XM_006719593.3:c.530C>T	XP_006719656.1:p.Ser177Phe
XM_011538731.2:c.449C>T	XP_011537033.1:p.Ser150Phe
XM_017019961.1:c.314C>T	XP_016875450.1:p.Ser105Phe
XM_017019962.2:c.-821C>T	XP_016875451.1:n.-821C>T
NM_024312.5:c.530C>T MANE Select	NP_077288.2:p.Ser177Phe