Canonical Allele Identifier: CA408946708
Gene: SPATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49905926G>C , CM000682.2:g.49905926G>C GRCh38
NC_000020.10:g.48522463G>C , CM000682.1:g.48522463G>C GRCh37
NC_000020.9:g.47955870G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289431.10:c.1256C>G MANE Select ENSP00000289431.5:p.Thr419Ser
ENST00000289431.9:c.1256C>G ENSP00000289431.5:p.Thr419Ser
ENST00000422556.1:c.1256C>G ENSP00000416799.1:p.Thr419Ser
NM_001135773.1:c.1256C>G NP_001129245.1:p.Thr419Ser
NM_006038.3:c.1256C>G NP_006029.1:p.Thr419Ser
XM_006723894.1:c.1256C>G XP_006723957.1:p.Thr419Ser
XM_011529116.1:c.1256C>G XP_011527418.1:p.Thr419Ser
NM_006038.4:c.1256C>G MANE Select NP_006029.1:p.Thr419Ser
NM_001135773.2:c.1256C>G NP_001129245.1:p.Thr419Ser