Canonical Allele Identifier: CA1420795296
Gene: SPATA16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173080809_173080825delinsAAAGTCCTGCCTTTTGC , CM000665.2:g.173080809_173080825delinsAAAGTCCTGCCTTTTGC GRCh38
NC_000003.11:g.172798599_172798615delinsAAAGTCCTGCCTTTTGC , CM000665.1:g.172798599_172798615delinsAAAGTCCTGCCTTTTGC GRCh37
NC_000003.10:g.174281293_174281309delinsAAAGTCCTGCCTTTTGC NCBI36
NG_021422.1:g.65444_65460delinsGCAAAAGGCAGGACTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000351008.4:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT MANE Select ENSP00000341765.3:n.613-31731_613-31715delinsGCAAAAGGCAGGACTT...
ENST00000351008.3:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT ENSP00000341765.3:n.613-31731_613-31715delinsGCAAAAGGCAGGACTT...
NM_031955.5:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT NP_114161.3:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT
XM_006713778.2:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT XP_006713841.1:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT
XM_011513222.1:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT XP_011511524.1:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT
XM_006713778.3:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT XP_006713841.1:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT
XM_017007308.2:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT XP_016862797.1:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT
NM_031955.6:c.613-31731_613-31715delinsGCAAAAGGCAGGACTTT MANE Select NP_114161.3:n.613-31731_613-31715delinsGCAAAAGGCAGGACTTT