Canonical Allele Identifier: CA2695208350

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683399_107683401del , CM000669.2:g.107683399_107683401del	GRCh38
NC_000007.13:g.107323844_107323846del , CM000669.1:g.107323844_107323846del	GRCh37
NC_000007.12:g.107111080_107111082del	NCBI36
NG_008489.1:g.27765_27767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.918+45_918+47del MANE Select	ENSP00000494017.1:n.918+45_918+47del
ENST00000265715.7:c.918+45_918+47del	ENSP00000265715.3:n.918+45_918+47del
NM_000441.1:c.918+45_918+47del	NP_000432.1:n.918+45_918+47del
XM_005250425.1:c.918+45_918+47del	XP_005250482.1:n.918+45_918+47del
XM_006716025.2:c.918+45_918+47del	XP_006716088.1:n.918+45_918+47del
XM_005250425.2:c.918+45_918+47del	XP_005250482.1:n.918+45_918+47del
XM_006716025.3:c.918+45_918+47del	XP_006716088.1:n.918+45_918+47del
XM_017012318.1:c.918+45_918+47del	XP_016867807.1:n.918+45_918+47del
NM_000441.2:c.918+45_918+47del MANE Select	NP_000432.1:n.918+45_918+47del