Canonical Allele Identifier: CA1732753108

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695970_107695971delinsTG , CM000669.2:g.107695970_107695971delinsTG	GRCh38
NC_000007.13:g.107336415_107336416delinsTG , CM000669.1:g.107336415_107336416delinsTG	GRCh37
NC_000007.12:g.107123651_107123652delinsTG	NCBI36
NG_008489.1:g.40336_40337delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1475_1476delinsTG MANE Select	ENSP00000494017.1:p.Leu492=
ENST00000644846.1:c.186_187delinsTG
ENST00000265715.7:c.1475_1476delinsTG	ENSP00000265715.3:p.Leu492=
ENST00000477350.5:n.322_323delinsTG
ENST00000480841.5:n.324_325delinsTG
ENST00000497446.5:n.490_491delinsTG
NM_000441.1:c.1475_1476delinsTG	NP_000432.1:p.Leu492=
XM_005250425.1:c.1475_1476delinsTG	XP_005250482.1:p.Leu492=
XM_005250425.2:c.1475_1476delinsTG	XP_005250482.1:p.Leu492=
XM_017012318.1:c.1397_1398delinsTG	XP_016867807.1:p.Leu466=
NM_000441.2:c.1475_1476delinsTG MANE Select	NP_000432.1:p.Leu492=