Canonical Allele Identifier: CA682765820

Gene: GNPTAB

Linked Data

• dbSNP Id: rs1434820244
• gnomAD v3: 12-101830731-C-T
• gnomAD v4: 12-101830731-C-T
• MyVariant Identifiers: chr12:g.102224509C>T (hg19) ; chr12:g.101830731C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830731C>T , CM000674.2:g.101830731C>T	GRCh38
NC_000012.11:g.102224509C>T , CM000674.1:g.102224509C>T	GRCh37
NC_000012.10:g.100748640C>T	NCBI36
NG_021243.1:g.5137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.-56G>A MANE Select	ENSP00000299314.7:n.-56G>A
ENST00000299314.11:c.-56G>A	ENSP00000299314.7:n.-56G>A
ENST00000392919.4:c.-56G>A	ENSP00000376651.4:n.-56G>A
ENST00000549940.5:c.-56G>A	ENSP00000449150.1:n.-56G>A
NM_024312.4:c.-56G>A	NP_077288.2:n.-56G>A
XM_006719593.2:c.-56G>A	XP_006719656.1:n.-56G>A
XM_006719593.3:c.-56G>A	XP_006719656.1:n.-56G>A
XM_017019961.1:c.-205G>A	XP_016875450.1:n.-205G>A
XM_017019962.2:c.-1406G>A	XP_016875451.1:n.-1406G>A
NM_024312.5:c.-56G>A MANE Select	NP_077288.2:n.-56G>A