Canonical Allele Identifier: CA1105618738

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1790574555
• gnomAD v4: 7-107662051-GGTTCTAGGAGCCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662054_107662067del , CM000669.2:g.107662054_107662067del	GRCh38
NC_000007.13:g.107302499_107302512del , CM000669.1:g.107302499_107302512del	GRCh37
NC_000007.12:g.107089735_107089748del	NCBI36
NG_008489.1:g.6420_6433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+249_164+262del MANE Select	ENSP00000494017.1:n.164+249_164+262del
ENST00000265715.7:c.164+249_164+262del	ENSP00000265715.3:n.164+249_164+262del
ENST00000440056.1:c.164+249_164+262del	ENSP00000394760.1:n.164+249_164+262del
NM_000441.1:c.164+249_164+262del	NP_000432.1:n.164+249_164+262del
XM_005250425.1:c.164+249_164+262del	XP_005250482.1:n.164+249_164+262del
XM_006716025.2:c.164+249_164+262del	XP_006716088.1:n.164+249_164+262del
XM_005250425.2:c.164+249_164+262del	XP_005250482.1:n.164+249_164+262del
XM_006716025.3:c.164+249_164+262del	XP_006716088.1:n.164+249_164+262del
XM_017012318.1:c.164+249_164+262del	XP_016867807.1:n.164+249_164+262del
NM_000441.2:c.164+249_164+262del MANE Select	NP_000432.1:n.164+249_164+262del