Canonical Allele Identifier: CA355537583
Gene: SPATA16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172737293C>G (hg19) chr3:g.173019503C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173019503C>G , CM000665.2:g.173019503C>G GRCh38
NC_000003.11:g.172737293C>G , CM000665.1:g.172737293C>G GRCh37
NC_000003.10:g.174219987C>G NCBI36
NG_021422.1:g.126766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351008.4:c.831G>C MANE Select ENSP00000341765.3:p.Arg277Ser
ENST00000351008.3:c.831G>C ENSP00000341765.3:p.Arg277Ser
NM_031955.5:c.831G>C NP_114161.3:p.Arg277Ser
XM_006713778.2:c.831G>C XP_006713841.1:p.Arg277Ser
XM_011513222.1:c.831G>C XP_011511524.1:p.Arg277Ser
XM_006713778.3:c.831G>C XP_006713841.1:p.Arg277Ser
XM_017007308.2:c.831G>C XP_016862797.1:p.Arg277Ser
NM_031955.6:c.831G>C MANE Select NP_114161.3:p.Arg277Ser
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