Canonical Allele Identifier: CA1056444714
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs1735266074
gnomAD v3: 3-173019397-T-G
gnomAD v4: 3-173019397-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173019397T>G , CM000665.2:g.173019397T>G GRCh38
NC_000003.11:g.172737187T>G , CM000665.1:g.172737187T>G GRCh37
NC_000003.10:g.174219881T>G NCBI36
NG_021422.1:g.126872A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.848+89A>C MANE Select ENSP00000341765.3:n.848+89A>C
ENST00000351008.3:c.848+89A>C ENSP00000341765.3:n.848+89A>C
NM_031955.5:c.848+89A>C NP_114161.3:n.848+89A>C
XM_006713778.2:c.848+89A>C XP_006713841.1:n.848+89A>C
XM_011513222.1:c.848+89A>C XP_011511524.1:n.848+89A>C
XM_006713778.3:c.848+89A>C XP_006713841.1:n.848+89A>C
XM_017007308.2:c.848+89A>C XP_016862797.1:n.848+89A>C
NM_031955.6:c.848+89A>C MANE Select NP_114161.3:n.848+89A>C
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