Canonical Allele Identifier: CA386487035

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101830638-C-T
• MyVariant Identifiers: chr12:g.102224416C>T (hg19) ; chr12:g.101830638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830638C>T , CM000674.2:g.101830638C>T	GRCh38
NC_000012.11:g.102224416C>T , CM000674.1:g.102224416C>T	GRCh37
NC_000012.10:g.100748547C>T	NCBI36
NG_021243.1:g.5230G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.38G>A MANE Select	ENSP00000299314.7:p.Cys13Tyr
ENST00000647144.1:n.26G>A
ENST00000299314.11:c.38G>A	ENSP00000299314.7:p.Cys13Tyr
ENST00000392919.4:c.38G>A	ENSP00000376651.4:p.Cys13Tyr
ENST00000549165.1:c.38G>A	ENSP00000450413.1:p.Cys13Tyr
ENST00000549940.5:c.38G>A	ENSP00000449150.1:p.Cys13Tyr
NM_024312.4:c.38G>A	NP_077288.2:p.Cys13Tyr
XM_006719593.2:c.38G>A	XP_006719656.1:p.Cys13Tyr
XM_006719593.3:c.38G>A	XP_006719656.1:p.Cys13Tyr
XM_017019961.1:c.-112G>A	XP_016875450.1:n.-112G>A
XM_017019962.2:c.-1313G>A	XP_016875451.1:n.-1313G>A
NM_024312.5:c.38G>A MANE Select	NP_077288.2:p.Cys13Tyr