Canonical Allele Identifier: CA2684466227

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107683635-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683636dup , CM000669.2:g.107683636dup	GRCh38
NC_000007.13:g.107324081dup , CM000669.1:g.107324081dup	GRCh37
NC_000007.12:g.107111317dup	NCBI36
NG_008489.1:g.28002dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1001+99dup MANE Select	ENSP00000494017.1:n.1001+99dup
ENST00000265715.7:c.1001+99dup	ENSP00000265715.3:n.1001+99dup
NM_000441.1:c.1001+99dup	NP_000432.1:n.1001+99dup
XM_005250425.1:c.1001+99dup	XP_005250482.1:n.1001+99dup
XM_006716025.2:c.1001+99dup	XP_006716088.1:n.1001+99dup
XM_005250425.2:c.1001+99dup	XP_005250482.1:n.1001+99dup
XM_006716025.3:c.1001+99dup	XP_006716088.1:n.1001+99dup
XM_017012318.1:c.1001+99dup	XP_016867807.1:n.1001+99dup
NM_000441.2:c.1001+99dup MANE Select	NP_000432.1:n.1001+99dup