Canonical Allele Identifier: CA2768879900

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977910_149977911insCACACCCAACAC , CM000667.2:g.149977910_149977911insCACACCCAACAC	GRCh38
NC_000005.9:g.149357473_149357474insCACACCCAACAC , CM000667.1:g.149357473_149357474insCACACCCAACAC	GRCh37
NC_000005.8:g.149337666_149337667insCACACCCAACAC	NCBI36
NG_007147.2:g.19028_19029insCACACCCAACAC , LRG_684:g.19028_19029insCACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.490_491insCACACCCAACAC
ENST00000286298.5:c.258_259insCACACCCAACAC MANE Select	ENSP00000286298.4:p.Lys86_Asn87insHisThrGlnHis
ENST00000286298.4:c.258_259insCACACCCAACAC	ENSP00000286298.4:p.Lys86_Asn87insHisThrGlnHis
NM_000112.3:c.258_259insCACACCCAACAC , LRG_684t1:c.258_259insCACACCCAACAC	NP_000103.2:p.Lys86_Asn87insHisThrGlnHis
XM_017009191.2:c.258_259insCACACCCAACAC	XP_016864680.1:p.Lys86_Asn87insHisThrGlnHis
NM_000112.4:c.258_259insCACACCCAACAC MANE Select	NP_000103.2:p.Lys86_Asn87insHisThrGlnHis