Canonical Allele Identifier: CA902698855
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs1173639144

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081124T>C , CM000665.2:g.173081124T>C GRCh38
NC_000003.11:g.172798914T>C , CM000665.1:g.172798914T>C GRCh37
NC_000003.10:g.174281608T>C NCBI36
NG_021422.1:g.65145A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351008.4:c.613-32030A>G MANE Select ENSP00000341765.3:n.613-32030A>G
ENST00000351008.3:c.613-32030A>G ENSP00000341765.3:n.613-32030A>G
NM_031955.5:c.613-32030A>G NP_114161.3:n.613-32030A>G
XM_006713778.2:c.613-32030A>G XP_006713841.1:n.613-32030A>G
XM_011513222.1:c.613-32030A>G XP_011511524.1:n.613-32030A>G
XM_006713778.3:c.613-32030A>G XP_006713841.1:n.613-32030A>G
XM_017007308.2:c.613-32030A>G XP_016862797.1:n.613-32030A>G
NM_031955.6:c.613-32030A>G MANE Select NP_114161.3:n.613-32030A>G