Canonical Allele Identifier: CA1420795390
Gene: SPATA16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081022C= , CM000665.2:g.173081022C= GRCh38
NC_000003.11:g.172798812C= , CM000665.1:g.172798812C= GRCh37
NC_000003.10:g.174281506C= NCBI36
NG_021422.1:g.65247G=

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31928G= MANE Select ENSP00000341765.3:n.613-31928G=
ENST00000351008.3:c.613-31928G= ENSP00000341765.3:n.613-31928G=
NM_031955.5:c.613-31928G= NP_114161.3:n.613-31928G=
XM_006713778.2:c.613-31928G= XP_006713841.1:n.613-31928G=
XM_011513222.1:c.613-31928G= XP_011511524.1:n.613-31928G=
XM_006713778.3:c.613-31928G= XP_006713841.1:n.613-31928G=
XM_017007308.2:c.613-31928G= XP_016862797.1:n.613-31928G=
NM_031955.6:c.613-31928G= MANE Select NP_114161.3:n.613-31928G=