Canonical Allele Identifier: CA1732741877

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683464_107683465delinsGC , CM000669.2:g.107683464_107683465delinsGC	GRCh38
NC_000007.13:g.107323909_107323910delinsGC , CM000669.1:g.107323909_107323910delinsGC	GRCh37
NC_000007.12:g.107111145_107111146delinsGC	NCBI36
NG_008489.1:g.27830_27831delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.928_929delinsGC MANE Select	ENSP00000494017.1:p.Ala310=
ENST00000265715.7:c.928_929delinsGC	ENSP00000265715.3:p.Ala310=
NM_000441.1:c.928_929delinsGC	NP_000432.1:p.Ala310=
XM_005250425.1:c.928_929delinsGC	XP_005250482.1:p.Ala310=
XM_006716025.2:c.928_929delinsGC	XP_006716088.1:p.Ala310=
XM_005250425.2:c.928_929delinsGC	XP_005250482.1:p.Ala310=
XM_006716025.3:c.928_929delinsGC	XP_006716088.1:p.Ala310=
XM_017012318.1:c.928_929delinsGC	XP_016867807.1:p.Ala310=
NM_000441.2:c.928_929delinsGC MANE Select	NP_000432.1:p.Ala310=