Canonical Allele Identifier: CA902698849

Gene: SPATA16

Linked Data

• dbSNP Id: rs1174996579
• gnomAD v3: 3-173081117-T-G
• gnomAD v4: 3-173081117-T-G
• MyVariant Identifiers: chr3:g.172798907T>G (hg19) ; chr3:g.173081117T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081117T>G , CM000665.2:g.173081117T>G	GRCh38
NC_000003.11:g.172798907T>G , CM000665.1:g.172798907T>G	GRCh37
NC_000003.10:g.174281601T>G	NCBI36
NG_021422.1:g.65152A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-32023A>C MANE Select	ENSP00000341765.3:n.613-32023A>C
ENST00000351008.3:c.613-32023A>C	ENSP00000341765.3:n.613-32023A>C
NM_031955.5:c.613-32023A>C	NP_114161.3:n.613-32023A>C
XM_006713778.2:c.613-32023A>C	XP_006713841.1:n.613-32023A>C
XM_011513222.1:c.613-32023A>C	XP_011511524.1:n.613-32023A>C
XM_006713778.3:c.613-32023A>C	XP_006713841.1:n.613-32023A>C
XM_017007308.2:c.613-32023A>C	XP_016862797.1:n.613-32023A>C
NM_031955.6:c.613-32023A>C MANE Select	NP_114161.3:n.613-32023A>C