Canonical Allele Identifier: CA6746850

Gene: GNPTAB

Linked Data

• dbSNP Id: rs772024246
• ExAC: 12:102179754 T / C
• gnomAD v2: 12-102179754-T-C
• gnomAD v4: 12-101785976-T-C
• MyVariant Identifiers: chr12:g.102179754T>C (hg19) ; chr12:g.101785976T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101785976T>C , CM000674.2:g.101785976T>C	GRCh38
NC_000012.11:g.102179754T>C , CM000674.1:g.102179754T>C	GRCh37
NC_000012.10:g.100703885T>C	NCBI36
NG_021243.1:g.49892A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.571+36A>G MANE Select	ENSP00000299314.7:n.571+36A>G
ENST00000299314.11:c.571+36A>G	ENSP00000299314.7:n.571+36A>G
ENST00000549940.5:c.571+36A>G	ENSP00000449150.1:n.571+36A>G
ENST00000550352.1:n.401A>G
ENST00000552681.1:c.205+36A>G	ENSP00000449217.1:n.205+36A>G
NM_024312.4:c.571+36A>G	NP_077288.2:n.571+36A>G
XM_006719593.2:c.571+36A>G	XP_006719656.1:n.571+36A>G
XM_011538731.1:c.490+36A>G	XP_011537033.1:n.490+36A>G
XM_006719593.3:c.571+36A>G	XP_006719656.1:n.571+36A>G
XM_011538731.2:c.490+36A>G	XP_011537033.1:n.490+36A>G
XM_017019961.1:c.355+36A>G	XP_016875450.1:n.355+36A>G
XM_017019962.2:c.-780+36A>G	XP_016875451.1:n.-780+36A>G
NM_024312.5:c.571+36A>G MANE Select	NP_077288.2:n.571+36A>G