Canonical Allele Identifier: CA1420768687

Gene: SPATA16

Linked Data

• dbSNP Id: rs1735266466

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173019420_173019421insATAA , CM000665.2:g.173019420_173019421insATAA	GRCh38
NC_000003.11:g.172737210_172737211insATAA , CM000665.1:g.172737210_172737211insATAA	GRCh37
NC_000003.10:g.174219904_174219905insATAA	NCBI36
NG_021422.1:g.126848_126849insTTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.848+65_848+66insTTAT MANE Select	ENSP00000341765.3:n.848+65_848+66insTTAT
ENST00000351008.3:c.848+65_848+66insTTAT	ENSP00000341765.3:n.848+65_848+66insTTAT
NM_031955.5:c.848+65_848+66insTTAT	NP_114161.3:n.848+65_848+66insTTAT
XM_006713778.2:c.848+65_848+66insTTAT	XP_006713841.1:n.848+65_848+66insTTAT
XM_011513222.1:c.848+65_848+66insTTAT	XP_011511524.1:n.848+65_848+66insTTAT
XM_006713778.3:c.848+65_848+66insTTAT	XP_006713841.1:n.848+65_848+66insTTAT
XM_017007308.2:c.848+65_848+66insTTAT	XP_016862797.1:n.848+65_848+66insTTAT
NM_031955.6:c.848+65_848+66insTTAT MANE Select	NP_114161.3:n.848+65_848+66insTTAT