Canonical Allele Identifier: CA2704590685

Gene: SPATA16

Linked Data

• dbSNP Id: rs2108313504

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081173G>A , CM000665.2:g.173081173G>A	GRCh38
NC_000003.11:g.172798963G>A , CM000665.1:g.172798963G>A	GRCh37
NC_000003.10:g.174281657G>A	NCBI36
NG_021422.1:g.65096C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-32079C>T MANE Select	ENSP00000341765.3:n.613-32079C>T
ENST00000351008.3:c.613-32079C>T	ENSP00000341765.3:n.613-32079C>T
NM_031955.5:c.613-32079C>T	NP_114161.3:n.613-32079C>T
XM_006713778.2:c.613-32079C>T	XP_006713841.1:n.613-32079C>T
XM_011513222.1:c.613-32079C>T	XP_011511524.1:n.613-32079C>T
XM_006713778.3:c.613-32079C>T	XP_006713841.1:n.613-32079C>T
XM_017007308.2:c.613-32079C>T	XP_016862797.1:n.613-32079C>T
NM_031955.6:c.613-32079C>T MANE Select	NP_114161.3:n.613-32079C>T