Canonical Allele Identifier: CA902698766

Gene: SPATA16

Linked Data

• dbSNP Id: rs1266459132
• MyVariant Identifiers: chr3:g.172798738A>T (hg19) ; chr3:g.173080948A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173080948A>T , CM000665.2:g.173080948A>T	GRCh38
NC_000003.11:g.172798738A>T , CM000665.1:g.172798738A>T	GRCh37
NC_000003.10:g.174281432A>T	NCBI36
NG_021422.1:g.65321T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-31854T>A MANE Select	ENSP00000341765.3:n.613-31854T>A
ENST00000351008.3:c.613-31854T>A	ENSP00000341765.3:n.613-31854T>A
NM_031955.5:c.613-31854T>A	NP_114161.3:n.613-31854T>A
XM_006713778.2:c.613-31854T>A	XP_006713841.1:n.613-31854T>A
XM_011513222.1:c.613-31854T>A	XP_011511524.1:n.613-31854T>A
XM_006713778.3:c.613-31854T>A	XP_006713841.1:n.613-31854T>A
XM_017007308.2:c.613-31854T>A	XP_016862797.1:n.613-31854T>A
NM_031955.6:c.613-31854T>A MANE Select	NP_114161.3:n.613-31854T>A