Canonical Allele Identifier: CA2684463351

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107675194-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675194_107675195insA , CM000669.2:g.107675194_107675195insA	GRCh38
NC_000007.13:g.107315639_107315640insA , CM000669.1:g.107315639_107315640insA	GRCh37
NC_000007.12:g.107102875_107102876insA	NCBI36
NG_008489.1:g.19560_19561insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+85_765+86insA MANE Select	ENSP00000494017.1:n.765+85_765+86insA
ENST00000265715.7:c.765+85_765+86insA	ENSP00000265715.3:n.765+85_765+86insA
NM_000441.1:c.765+85_765+86insA	NP_000432.1:n.765+85_765+86insA
XM_005250425.1:c.765+85_765+86insA	XP_005250482.1:n.765+85_765+86insA
XM_006716025.2:c.765+85_765+86insA	XP_006716088.1:n.765+85_765+86insA
XM_005250425.2:c.765+85_765+86insA	XP_005250482.1:n.765+85_765+86insA
XM_006716025.3:c.765+85_765+86insA	XP_006716088.1:n.765+85_765+86insA
XM_017012318.1:c.765+85_765+86insA	XP_016867807.1:n.765+85_765+86insA
NM_000441.2:c.765+85_765+86insA MANE Select	NP_000432.1:n.765+85_765+86insA