Canonical Allele Identifier: CA2684465734

Gene: SLC26A4 SLC26A4-AS1

Linked Data

• gnomAD v4: 7-107661760-TGCAGGAGCGCAAGACGCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661761_107661779del , CM000669.2:g.107661761_107661779del	GRCh38
NC_000007.13:g.107302206_107302224del , CM000669.1:g.107302206_107302224del	GRCh37
NC_000007.12:g.107089442_107089460del	NCBI36
NG_008489.1:g.6127_6145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.120_138del (SLC26A4) MANE Select	ENSP00000494017.1:p.Gln41GlyfsTer19
ENST00000265715.7:c.120_138del (SLC26A4)	ENSP00000265715.3:p.Gln41GlyfsTer19
ENST00000440056.1:c.120_138del (SLC26A4)	ENSP00000394760.1:p.Gln41GlyfsTer19
NM_000441.1:c.120_138del (SLC26A4)	NP_000432.1:p.Gln41GlyfsTer19
NR_028137.1:n.20_38del (SLC26A4-AS1)
XM_005250425.1:c.120_138del (SLC26A4)	XP_005250482.1:p.Gln41GlyfsTer19
XM_006716025.2:c.120_138del (SLC26A4)	XP_006716088.1:p.Gln41GlyfsTer19
XM_005250425.2:c.120_138del (SLC26A4)	XP_005250482.1:p.Gln41GlyfsTer19
XM_006716025.3:c.120_138del (SLC26A4)	XP_006716088.1:p.Gln41GlyfsTer19
XM_017012318.1:c.120_138del (SLC26A4)	XP_016867807.1:p.Gln41GlyfsTer19
NM_000441.2:c.120_138del (SLC26A4) MANE Select	NP_000432.1:p.Gln41GlyfsTer19