Canonical Allele Identifier: CA2740094129
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937372
ClinVar RCV Id: RCV003791562

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977893del , CM000667.2:g.149977893del GRCh38
NC_000005.9:g.149357456del , CM000667.1:g.149357456del GRCh37
NC_000005.8:g.149337649del NCBI36
NG_007147.2:g.19011del , LRG_684:g.19011del

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.473del
ENST00000286298.5:c.241del MANE Select ENSP00000286298.4:p.Ser81ValfsTer8
ENST00000286298.4:c.241del ENSP00000286298.4:p.Ser81ValfsTer8
NM_000112.3:c.241del , LRG_684t1:c.241del NP_000103.2:p.Ser81ValfsTer8
XM_017009191.2:c.241del XP_016864680.1:p.Ser81ValfsTer8
NM_000112.4:c.241del MANE Select NP_000103.2:p.Ser81ValfsTer8