Canonical Allele Identifier: CA88219499
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs987832140

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081089C>G , CM000665.2:g.173081089C>G GRCh38
NC_000003.11:g.172798879C>G , CM000665.1:g.172798879C>G GRCh37
NC_000003.10:g.174281573C>G NCBI36
NG_021422.1:g.65180G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351008.4:c.613-31995G>C MANE Select ENSP00000341765.3:n.613-31995G>C
ENST00000351008.3:c.613-31995G>C ENSP00000341765.3:n.613-31995G>C
NM_031955.5:c.613-31995G>C NP_114161.3:n.613-31995G>C
XM_006713778.2:c.613-31995G>C XP_006713841.1:n.613-31995G>C
XM_011513222.1:c.613-31995G>C XP_011511524.1:n.613-31995G>C
XM_006713778.3:c.613-31995G>C XP_006713841.1:n.613-31995G>C
XM_017007308.2:c.613-31995G>C XP_016862797.1:n.613-31995G>C
NM_031955.6:c.613-31995G>C MANE Select NP_114161.3:n.613-31995G>C