Canonical Allele Identifier: CA1420768677
Gene: SPATA16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173019387A= , CM000665.2:g.173019387A= GRCh38
NC_000003.11:g.172737177A= , CM000665.1:g.172737177A= GRCh37
NC_000003.10:g.174219871A= NCBI36
NG_021422.1:g.126882T=

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.848+99T= MANE Select ENSP00000341765.3:n.848+99T=
ENST00000351008.3:c.848+99T= ENSP00000341765.3:n.848+99T=
NM_031955.5:c.848+99T= NP_114161.3:n.848+99T=
XM_006713778.2:c.848+99T= XP_006713841.1:n.848+99T=
XM_011513222.1:c.848+99T= XP_011511524.1:n.848+99T=
XM_006713778.3:c.848+99T= XP_006713841.1:n.848+99T=
XM_017007308.2:c.848+99T= XP_016862797.1:n.848+99T=
NM_031955.6:c.848+99T= MANE Select NP_114161.3:n.848+99T=
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