Canonical Allele Identifier: CA2668589015

Gene: SPATA16

Linked Data

• gnomAD v4: 3-173019404-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173019406_173019407del , CM000665.2:g.173019406_173019407del	GRCh38
NC_000003.11:g.172737196_172737197del , CM000665.1:g.172737196_172737197del	GRCh37
NC_000003.10:g.174219890_174219891del	NCBI36
NG_021422.1:g.126863_126864del

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.848+80_848+81del MANE Select	ENSP00000341765.3:n.848+80_848+81del
ENST00000351008.3:c.848+80_848+81del	ENSP00000341765.3:n.848+80_848+81del
NM_031955.5:c.848+80_848+81del	NP_114161.3:n.848+80_848+81del
XM_006713778.2:c.848+80_848+81del	XP_006713841.1:n.848+80_848+81del
XM_011513222.1:c.848+80_848+81del	XP_011511524.1:n.848+80_848+81del
XM_006713778.3:c.848+80_848+81del	XP_006713841.1:n.848+80_848+81del
XM_017007308.2:c.848+80_848+81del	XP_016862797.1:n.848+80_848+81del
NM_031955.6:c.848+80_848+81del MANE Select	NP_114161.3:n.848+80_848+81del