Canonical Allele Identifier: CA2201615501
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362945_1362972delinsCACTCGCCACCTGTGGGTCCAGGTGAGG , CM000678.2:g.1362945_1362972delinsCACTCGCCACCTGTGGGTCCAGGTGAGG GRCh38
NC_000016.9:g.1412946_1412973delinsCACTCGCCACCTGTGGGTCCAGGTGAGG , CM000678.1:g.1412946_1412973delinsCACTCGCCACCTGTGGGTCCAGGTGAGG GRCh37
NC_000016.8:g.1352947_1352974delinsCACTCGCCACCTGTGGGTCCAGGTGAGG NCBI36
NG_016985.1:g.16047_16074delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
NG_033129.1:g.56733_56760delinsCCTCACCTGGACCCACAGGTGGCGAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.922+39_923-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000529110.2:c.907+39_908-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG ENSP00000435349.2:n.907+39_908-25delinsCACTCGCCACCTGTGGGTCCAG...
ENST00000529957.6:n.881+39_882-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000683366.1:c.*555+39_*556-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG ENSP00000507283.1:n.*555+39_*556-25delinsCACTCGCCACCTGTGGGTCC...
ENST00000683887.1:c.871+39_872-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG ENSP00000506886.1:n.871+39_872-25delinsCACTCGCCACCTGTGGGTCCAG...
ENST00000684100.1:n.817+39_818-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000684126.1:n.957+39_958-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000684688.1:n.1448+39_1449-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000204679.9:c.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG MANE Select ENSP00000204679.4:n.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAG...
ENST00000204679.8:c.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG ENSP00000204679.4:n.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAG...
ENST00000527076.1:n.2046+39_2047-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
ENST00000527168.5:n.990+39_991-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG
NM_032520.4:c.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG NP_115909.1:n.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG...
XM_017023782.1:c.871+39_872-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG XP_016879271.1:n.871+39_872-25delinsCACTCGCCACCTGTGGGTCCAGGTG...
XM_017023783.1:c.463+39_464-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG XP_016879272.1:n.463+39_464-25delinsCACTCGCCACCTGTGGGTCCAGGTG...
NM_032520.5:c.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG MANE Select NP_115909.1:n.823+39_824-25delinsCACTCGCCACCTGTGGGTCCAGGTGAGG...