Canonical Allele Identifier: CA6746866
Gene: GNPTAB HGNC NCBI

Linked Data

dbSNP Id: rs745555516

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101786062T>C , CM000674.2:g.101786062T>C GRCh38
NC_000012.11:g.102179840T>C , CM000674.1:g.102179840T>C GRCh37
NC_000012.10:g.100703971T>C NCBI36
NG_021243.1:g.49806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.521A>G MANE Select ENSP00000299314.7:p.Lys174Arg
ENST00000299314.11:c.521A>G ENSP00000299314.7:p.Lys174Arg
ENST00000549940.5:c.521A>G ENSP00000449150.1:p.Lys174Arg
ENST00000550352.1:n.315A>G
ENST00000552681.1:c.155A>G ENSP00000449217.1:p.Lys52Arg
NM_024312.4:c.521A>G NP_077288.2:p.Lys174Arg
XM_006719593.2:c.521A>G XP_006719656.1:p.Lys174Arg
XM_011538731.1:c.440A>G XP_011537033.1:p.Lys147Arg
XM_006719593.3:c.521A>G XP_006719656.1:p.Lys174Arg
XM_011538731.2:c.440A>G XP_011537033.1:p.Lys147Arg
XM_017019961.1:c.305A>G XP_016875450.1:p.Lys102Arg
XM_017019962.2:c.-830A>G XP_016875451.1:n.-830A>G
NM_024312.5:c.521A>G MANE Select NP_077288.2:p.Lys174Arg