Canonical Allele Identifier: CA2684466521

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107690126-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690128del , CM000669.2:g.107690128del	GRCh38
NC_000007.13:g.107330573del , CM000669.1:g.107330573del	GRCh37
NC_000007.12:g.107117809del	NCBI36
NG_008489.1:g.34494del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1154del MANE Select	ENSP00000494017.1:p.Phe385SerfsTer?
ENST00000265715.7:c.1154del	ENSP00000265715.3:p.Phe385SerfsTer?
NM_000441.1:c.1154del	NP_000432.1:p.Phe385SerfsTer?
XM_005250425.1:c.1154del	XP_005250482.1:p.Phe385SerfsTer?
XM_006716025.2:c.1154del	XP_006716088.1:p.Phe385SerfsTer?
XM_005250425.2:c.1154del	XP_005250482.1:p.Phe385SerfsTer?
XM_006716025.3:c.1154del	XP_006716088.1:p.Phe385SerfsTer?
XM_017012318.1:c.1154del	XP_016867807.1:p.Phe385SerfsTer?
NM_000441.2:c.1154del MANE Select	NP_000432.1:p.Phe385SerfsTer?