Canonical Allele Identifier: CA2684459844

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107672189-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107672190del , CM000669.2:g.107672190del	GRCh38
NC_000007.13:g.107312635del , CM000669.1:g.107312635del	GRCh37
NC_000007.12:g.107099871del	NCBI36
NG_008489.1:g.16556del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.357del MANE Select	ENSP00000494017.1:p.Ala120LeufsTer6
ENST00000265715.7:c.357del	ENSP00000265715.3:p.Ala120LeufsTer6
ENST00000440056.1:c.357del	ENSP00000394760.1:p.Ala120LeufsTer6
NM_000441.1:c.357del	NP_000432.1:p.Ala120LeufsTer6
XM_005250425.1:c.357del	XP_005250482.1:p.Ala120LeufsTer6
XM_006716025.2:c.357del	XP_006716088.1:p.Ala120LeufsTer6
XM_005250425.2:c.357del	XP_005250482.1:p.Ala120LeufsTer6
XM_006716025.3:c.357del	XP_006716088.1:p.Ala120LeufsTer6
XM_017012318.1:c.357del	XP_016867807.1:p.Ala120LeufsTer6
NM_000441.2:c.357del MANE Select	NP_000432.1:p.Ala120LeufsTer6