Canonical Allele Identifier: CA15295877
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs1878007

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081010G>A , CM000665.2:g.173081010G>A GRCh38
NC_000003.11:g.172798800G>A , CM000665.1:g.172798800G>A GRCh37
NC_000003.10:g.174281494G>A NCBI36
NG_021422.1:g.65259C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31916C>T MANE Select ENSP00000341765.3:n.613-31916C>T
ENST00000351008.3:c.613-31916C>T ENSP00000341765.3:n.613-31916C>T
NM_031955.5:c.613-31916C>T NP_114161.3:n.613-31916C>T
XM_006713778.2:c.613-31916C>T XP_006713841.1:n.613-31916C>T
XM_011513222.1:c.613-31916C>T XP_011511524.1:n.613-31916C>T
XM_006713778.3:c.613-31916C>T XP_006713841.1:n.613-31916C>T
XM_017007308.2:c.613-31916C>T XP_016862797.1:n.613-31916C>T
NM_031955.6:c.613-31916C>T MANE Select NP_114161.3:n.613-31916C>T