Canonical Allele Identifier: CA902698855

Gene: SPATA16

Linked Data

• dbSNP Id: rs1173639144
• gnomAD v3: 3-173081124-T-C
• gnomAD v4: 3-173081124-T-C
• MyVariant Identifiers: chr3:g.172798914T>C (hg19) ; chr3:g.173081124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081124T>C , CM000665.2:g.173081124T>C	GRCh38
NC_000003.11:g.172798914T>C , CM000665.1:g.172798914T>C	GRCh37
NC_000003.10:g.174281608T>C	NCBI36
NG_021422.1:g.65145A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-32030A>G MANE Select	ENSP00000341765.3:n.613-32030A>G
ENST00000351008.3:c.613-32030A>G	ENSP00000341765.3:n.613-32030A>G
NM_031955.5:c.613-32030A>G	NP_114161.3:n.613-32030A>G
XM_006713778.2:c.613-32030A>G	XP_006713841.1:n.613-32030A>G
XM_011513222.1:c.613-32030A>G	XP_011511524.1:n.613-32030A>G
XM_006713778.3:c.613-32030A>G	XP_006713841.1:n.613-32030A>G
XM_017007308.2:c.613-32030A>G	XP_016862797.1:n.613-32030A>G
NM_031955.6:c.613-32030A>G MANE Select	NP_114161.3:n.613-32030A>G