Canonical Allele Identifier: CA2695208248

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663366del , CM000669.2:g.107663366del	GRCh38
NC_000007.13:g.107303811del , CM000669.1:g.107303811del	GRCh37
NC_000007.12:g.107091047del	NCBI36
NG_008489.1:g.7732del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.235del MANE Select	ENSP00000494017.1:p.Arg79GlufsTer18
ENST00000265715.7:c.235del	ENSP00000265715.3:p.Arg79GlufsTer18
ENST00000440056.1:c.235del	ENSP00000394760.1:p.Arg79GlufsTer18
NM_000441.1:c.235del	NP_000432.1:p.Arg79GlufsTer18
XM_005250425.1:c.235del	XP_005250482.1:p.Arg79GlufsTer18
XM_006716025.2:c.235del	XP_006716088.1:p.Arg79GlufsTer18
XM_005250425.2:c.235del	XP_005250482.1:p.Arg79GlufsTer18
XM_006716025.3:c.235del	XP_006716088.1:p.Arg79GlufsTer18
XM_017012318.1:c.235del	XP_016867807.1:p.Arg79GlufsTer18
NM_000441.2:c.235del MANE Select	NP_000432.1:p.Arg79GlufsTer18