Canonical Allele Identifier: CA1619252907
Gene: GPANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31662176A>T , CM000668.2:g.31662176A>T GRCh38
NC_000006.11:g.31629953A>T , CM000668.1:g.31629953A>T GRCh37
NC_000006.10:g.31737932A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375896.9:c.*90T>A MANE Select ENSP00000365060.4:n.*90T>A
ENST00000375893.6:c.*90T>A ENSP00000365057.2:n.*90T>A
ENST00000375895.6:c.*90T>A ENSP00000365059.2:n.*90T>A
ENST00000375896.8:c.*90T>A ENSP00000365060.4:n.*90T>A
ENST00000375900.8:c.*90T>A ENSP00000365065.4:n.*90T>A
ENST00000375906.5:c.*90T>A ENSP00000365071.1:n.*90T>A
NM_001199237.1:c.*90T>A NP_001186166.1:n.*90T>A
NM_001199238.1:c.*90T>A NP_001186167.1:n.*90T>A
NM_001199239.1:c.*90T>A NP_001186168.1:n.*90T>A
NM_001199240.1:c.*90T>A NP_001186169.1:n.*90T>A
NM_033177.3:c.*90T>A NP_149417.1:n.*90T>A
XM_005249403.2:c.*90T>A XP_005249460.1:n.*90T>A
XM_006715204.1:c.*90T>A XP_006715267.1:n.*90T>A
XM_011514909.1:c.*90T>A XP_011513211.1:n.*90T>A
XM_011514910.1:c.*90T>A XP_011513212.1:n.*90T>A
XM_005249403.3:c.*90T>A XP_005249460.1:n.*90T>A
XM_024446548.1:c.*90T>A XP_024302316.1:n.*90T>A
XM_024446549.1:c.*90T>A XP_024302317.1:n.*90T>A
NM_033177.4:c.*90T>A MANE Select NP_149417.1:n.*90T>A