Canonical Allele Identifier: CA2843648152

Gene: SLC26A4 SLC26A4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661783del , CM000669.2:g.107661783del	GRCh38
NC_000007.13:g.107302228del , CM000669.1:g.107302228del	GRCh37
NC_000007.12:g.107089464del	NCBI36
NG_008489.1:g.6149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.142del (SLC26A4) MANE Select	ENSP00000494017.1:p.Glu48ArgfsTer18
ENST00000265715.7:c.142del (SLC26A4)	ENSP00000265715.3:p.Glu48ArgfsTer18
ENST00000440056.1:c.142del (SLC26A4)	ENSP00000394760.1:p.Glu48ArgfsTer18
NM_000441.1:c.142del (SLC26A4)	NP_000432.1:p.Glu48ArgfsTer18
NR_028137.1:n.18del (SLC26A4-AS1)
XM_005250425.1:c.142del (SLC26A4)	XP_005250482.1:p.Glu48ArgfsTer18
XM_006716025.2:c.142del (SLC26A4)	XP_006716088.1:p.Glu48ArgfsTer18
XM_005250425.2:c.142del (SLC26A4)	XP_005250482.1:p.Glu48ArgfsTer18
XM_006716025.3:c.142del (SLC26A4)	XP_006716088.1:p.Glu48ArgfsTer18
XM_017012318.1:c.142del (SLC26A4)	XP_016867807.1:p.Glu48ArgfsTer18
NM_000441.2:c.142del (SLC26A4) MANE Select	NP_000432.1:p.Glu48ArgfsTer18