Canonical Allele Identifier: CA386299209

Gene: GNPTAB

Linked Data

• dbSNP Id: rs1566074203
• gnomAD v2: 12-102158690-T-C
• gnomAD v4: 12-101764912-T-C
• MyVariant Identifiers: chr12:g.102158690T>C (hg19) ; chr12:g.101764912T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101764912T>C , CM000674.2:g.101764912T>C	GRCh38
NC_000012.11:g.102158690T>C , CM000674.1:g.102158690T>C	GRCh37
NC_000012.10:g.100682821T>C	NCBI36
NG_021243.1:g.70956A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2005A>G MANE Select	ENSP00000299314.7:p.Ile669Val
ENST00000299314.11:c.2005A>G	ENSP00000299314.7:p.Ile669Val
NM_024312.4:c.2005A>G	NP_077288.2:p.Ile669Val
XM_006719593.2:c.2005A>G	XP_006719656.1:p.Ile669Val
XM_011538731.1:c.1924A>G	XP_011537033.1:p.Ile642Val
XM_006719593.3:c.2005A>G	XP_006719656.1:p.Ile669Val
XM_011538731.2:c.1924A>G	XP_011537033.1:p.Ile642Val
XM_017019961.1:c.1789A>G	XP_016875450.1:p.Ile597Val
XM_017019962.2:c.778A>G	XP_016875451.1:p.Ile260Val
NM_024312.5:c.2005A>G MANE Select	NP_077288.2:p.Ile669Val