Canonical Allele Identifier: CA1732741943

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683494_107683495delinsGA , CM000669.2:g.107683494_107683495delinsGA	GRCh38
NC_000007.13:g.107323939_107323940delinsGA , CM000669.1:g.107323939_107323940delinsGA	GRCh37
NC_000007.12:g.107111175_107111176delinsGA	NCBI36
NG_008489.1:g.27860_27861delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.958_959delinsGA MANE Select	ENSP00000494017.1:p.Glu320=
ENST00000265715.7:c.958_959delinsGA	ENSP00000265715.3:p.Glu320=
NM_000441.1:c.958_959delinsGA	NP_000432.1:p.Glu320=
XM_005250425.1:c.958_959delinsGA	XP_005250482.1:p.Glu320=
XM_006716025.2:c.958_959delinsGA	XP_006716088.1:p.Glu320=
XM_005250425.2:c.958_959delinsGA	XP_005250482.1:p.Glu320=
XM_006716025.3:c.958_959delinsGA	XP_006716088.1:p.Glu320=
XM_017012318.1:c.958_959delinsGA	XP_016867807.1:p.Glu320=
NM_000441.2:c.958_959delinsGA MANE Select	NP_000432.1:p.Glu320=