Canonical Allele Identifier: CA2201592060
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1351964_1351974del , CM000678.2:g.1351964_1351974del GRCh38
NC_000016.9:g.1401965_1401975del , CM000678.1:g.1401965_1401975del GRCh37
NC_000016.8:g.1341966_1341976del NCBI36
NG_016985.1:g.5066_5076del

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.19_29del
ENST00000683366.1:c.-2_9del
ENST00000683887.1:c.-2_9del
ENST00000204679.9:c.-2_9del
ENST00000204679.8:c.-2_9del
ENST00000526820.5:c.-2_9del
ENST00000527137.2:c.-2_9del
ENST00000527168.5:n.11_21del
ENST00000527876.5:c.-2_9del
ENST00000529957.5:n.19_29del
ENST00000534197.5:n.17_27del
NM_032520.4:c.-2_9del
XM_017023782.1:c.-2_9del
NM_032520.5:c.-2_9del