Canonical Allele Identifier: CA4432645

Gene: SLC26A4

Linked Data

• dbSNP Id: rs771549055
• ExAC: 7:107324006 AC / A
• gnomAD v2: 7-107324006-AC-A
• gnomAD v4: 7-107683561-AC-A
• MyVariant Identifiers: chr7:g.107324007del (hg19) ; chr7:g.107683562del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683562del , CM000669.2:g.107683562del	GRCh38
NC_000007.13:g.107324007del , CM000669.1:g.107324007del	GRCh37
NC_000007.12:g.107111243del	NCBI36
NG_008489.1:g.27928del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1001+25del MANE Select	ENSP00000494017.1:n.1001+25del
ENST00000265715.7:c.1001+25del	ENSP00000265715.3:n.1001+25del
NM_000441.1:c.1001+25del	NP_000432.1:n.1001+25del
XM_005250425.1:c.1001+25del	XP_005250482.1:n.1001+25del
XM_006716025.2:c.1001+25del	XP_006716088.1:n.1001+25del
XM_005250425.2:c.1001+25del	XP_005250482.1:n.1001+25del
XM_006716025.3:c.1001+25del	XP_006716088.1:n.1001+25del
XM_017012318.1:c.1001+25del	XP_016867807.1:n.1001+25del
NM_000441.2:c.1001+25del MANE Select	NP_000432.1:n.1001+25del