Canonical Allele Identifier: CA548089184

Gene: SPATA16

Linked Data

• dbSNP Id: rs1175681440
• gnomAD v2: 3-172798932-TGAGA-T
• MyVariant Identifiers: chr3:g.172798933_172798936del (hg19) ; chr3:g.173081143_173081146del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081145_173081148del , CM000665.2:g.173081145_173081148del	GRCh38
NC_000003.11:g.172798935_172798938del , CM000665.1:g.172798935_172798938del	GRCh37
NC_000003.10:g.174281629_174281632del	NCBI36
NG_021422.1:g.65123_65126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-32052_613-32049del MANE Select	ENSP00000341765.3:n.613-32052_613-32049del
ENST00000351008.3:c.613-32052_613-32049del	ENSP00000341765.3:n.613-32052_613-32049del
NM_031955.5:c.613-32052_613-32049del	NP_114161.3:n.613-32052_613-32049del
XM_006713778.2:c.613-32052_613-32049del	XP_006713841.1:n.613-32052_613-32049del
XM_011513222.1:c.613-32052_613-32049del	XP_011511524.1:n.613-32052_613-32049del
XM_006713778.3:c.613-32052_613-32049del	XP_006713841.1:n.613-32052_613-32049del
XM_017007308.2:c.613-32052_613-32049del	XP_016862797.1:n.613-32052_613-32049del
NM_031955.6:c.613-32052_613-32049del MANE Select	NP_114161.3:n.613-32052_613-32049del