Canonical Allele Identifier: CA481320737

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101770490-A-C
• MyVariant Identifiers: chr12:g.102164268A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770490A>C , CM000674.2:g.101770490A>C	GRCh38
NC_000012.11:g.102164268A>C , CM000674.1:g.102164268A>C	GRCh37
NC_000012.10:g.100688399A>C	NCBI36
NG_021243.1:g.65378T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1029T>G MANE Select	ENSP00000299314.7:p.Val343=
ENST00000299314.11:c.1029T>G	ENSP00000299314.7:p.Val343=
ENST00000549940.5:c.1029T>G	ENSP00000449150.1:p.Val343=
NM_024312.4:c.1029T>G	NP_077288.2:p.Val343=
XM_006719593.2:c.1029T>G	XP_006719656.1:p.Val343=
XM_011538731.1:c.948T>G	XP_011537033.1:p.Val316=
XM_006719593.3:c.1029T>G	XP_006719656.1:p.Val343=
XM_011538731.2:c.948T>G	XP_011537033.1:p.Val316=
XM_017019961.1:c.813T>G	XP_016875450.1:p.Val271=
XM_017019962.2:c.-199T>G	XP_016875451.1:n.-199T>G
NM_024312.5:c.1029T>G MANE Select	NP_077288.2:p.Val343=