Canonical Allele Identifier: CA242462661

Gene: GNPTAB

Linked Data

• dbSNP Id: rs988926226
• gnomAD v2: 12-102164360-T-C
• gnomAD v4: 12-101770582-T-C
• MyVariant Identifiers: chr12:g.102164360T>C (hg19) ; chr12:g.101770582T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770582T>C , CM000674.2:g.101770582T>C	GRCh38
NC_000012.11:g.102164360T>C , CM000674.1:g.102164360T>C	GRCh37
NC_000012.10:g.100688491T>C	NCBI36
NG_021243.1:g.65286A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.937A>G MANE Select	ENSP00000299314.7:p.Lys313Glu
ENST00000299314.11:c.937A>G	ENSP00000299314.7:p.Lys313Glu
ENST00000549940.5:c.937A>G	ENSP00000449150.1:p.Lys313Glu
NM_024312.4:c.937A>G	NP_077288.2:p.Lys313Glu
XM_006719593.2:c.937A>G	XP_006719656.1:p.Lys313Glu
XM_011538731.1:c.856A>G	XP_011537033.1:p.Lys286Glu
XM_006719593.3:c.937A>G	XP_006719656.1:p.Lys313Glu
XM_011538731.2:c.856A>G	XP_011537033.1:p.Lys286Glu
XM_017019961.1:c.721A>G	XP_016875450.1:p.Lys241Glu
XM_017019962.2:c.-291A>G	XP_016875451.1:n.-291A>G
NM_024312.5:c.937A>G MANE Select	NP_077288.2:p.Lys313Glu