Canonical Allele Identifier: CA1732747399

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107689182_107689195delinsCACCATCGATGGGA , CM000669.2:g.107689182_107689195delinsCACCATCGATGGGA	GRCh38
NC_000007.13:g.107329627_107329640delinsCACCATCGATGGGA , CM000669.1:g.107329627_107329640delinsCACCATCGATGGGA	GRCh37
NC_000007.12:g.107116863_107116876delinsCACCATCGATGGGA	NCBI36
NG_008489.1:g.33548_33561delinsCACCATCGATGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1131_1144delinsCACCATCGATGGGA MANE Select	ENSP00000494017.1:p.Tyr377=
ENST00000265715.7:c.1131_1144delinsCACCATCGATGGGA	ENSP00000265715.3:p.Tyr377=
NM_000441.1:c.1131_1144delinsCACCATCGATGGGA	NP_000432.1:p.Tyr377=
XM_005250425.1:c.1131_1144delinsCACCATCGATGGGA	XP_005250482.1:p.Tyr377=
XM_006716025.2:c.1131_1144delinsCACCATCGATGGGA	XP_006716088.1:p.Tyr377=
XM_005250425.2:c.1131_1144delinsCACCATCGATGGGA	XP_005250482.1:p.Tyr377=
XM_006716025.3:c.1131_1144delinsCACCATCGATGGGA	XP_006716088.1:p.Tyr377=
XM_017012318.1:c.1131_1144delinsCACCATCGATGGGA	XP_016867807.1:p.Tyr377=
NM_000441.2:c.1131_1144delinsCACCATCGATGGGA MANE Select	NP_000432.1:p.Tyr377=