Canonical Allele Identifier: CA1420795354
Gene: SPATA16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173080964_173080965delinsGC , CM000665.2:g.173080964_173080965delinsGC GRCh38
NC_000003.11:g.172798754_172798755delinsGC , CM000665.1:g.172798754_172798755delinsGC GRCh37
NC_000003.10:g.174281448_174281449delinsGC NCBI36
NG_021422.1:g.65304_65305delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31871_613-31870delinsGC MANE Select ENSP00000341765.3:n.613-31871_613-31870de...
ENST00000351008.3:c.613-31871_613-31870delinsGC ENSP00000341765.3:n.613-31871_613-31870de...
NM_031955.5:c.613-31871_613-31870delinsGC NP_114161.3:n.613-31871_613-31870delinsGC...
XM_006713778.2:c.613-31871_613-31870delinsGC XP_006713841.1:n.613-31871_613-31870delin...
XM_011513222.1:c.613-31871_613-31870delinsGC XP_011511524.1:n.613-31871_613-31870delin...
XM_006713778.3:c.613-31871_613-31870delinsGC XP_006713841.1:n.613-31871_613-31870delin...
XM_017007308.2:c.613-31871_613-31870delinsGC XP_016862797.1:n.613-31871_613-31870delin...
NM_031955.6:c.613-31871_613-31870delinsGC MANE Select NP_114161.3:n.613-31871_613-31870delinsGC...