Canonical Allele Identifier: CA1732741741

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683352_107683353delinsGT , CM000669.2:g.107683352_107683353delinsGT	GRCh38
NC_000007.13:g.107323797_107323798delinsGT , CM000669.1:g.107323797_107323798delinsGT	GRCh37
NC_000007.12:g.107111033_107111034delinsGT	NCBI36
NG_008489.1:g.27718_27719delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.916_917delinsGT MANE Select	ENSP00000494017.1:p.Val306=
ENST00000265715.7:c.916_917delinsGT	ENSP00000265715.3:p.Val306=
NM_000441.1:c.916_917delinsGT	NP_000432.1:p.Val306=
XM_005250425.1:c.916_917delinsGT	XP_005250482.1:p.Val306=
XM_006716025.2:c.916_917delinsGT	XP_006716088.1:p.Val306=
XM_005250425.2:c.916_917delinsGT	XP_005250482.1:p.Val306=
XM_006716025.3:c.916_917delinsGT	XP_006716088.1:p.Val306=
XM_017012318.1:c.916_917delinsGT	XP_016867807.1:p.Val306=
NM_000441.2:c.916_917delinsGT MANE Select	NP_000432.1:p.Val306=