Canonical Allele Identifier: CA1420795377
Gene: SPATA16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173080998T= , CM000665.2:g.173080998T= GRCh38
NC_000003.11:g.172798788T= , CM000665.1:g.172798788T= GRCh37
NC_000003.10:g.174281482T= NCBI36
NG_021422.1:g.65271A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351008.4:c.613-31904A= MANE Select ENSP00000341765.3:n.613-31904A=
ENST00000351008.3:c.613-31904A= ENSP00000341765.3:n.613-31904A=
NM_031955.5:c.613-31904A= NP_114161.3:n.613-31904A=
XM_006713778.2:c.613-31904A= XP_006713841.1:n.613-31904A=
XM_011513222.1:c.613-31904A= XP_011511524.1:n.613-31904A=
XM_006713778.3:c.613-31904A= XP_006713841.1:n.613-31904A=
XM_017007308.2:c.613-31904A= XP_016862797.1:n.613-31904A=
NM_031955.6:c.613-31904A= MANE Select NP_114161.3:n.613-31904A=
Search 100 bp 5'
Search 100 bp 3'