Canonical Allele Identifier: CA831183309

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1415657045
• gnomAD v3: 7-107695815-AAG-A
• gnomAD v4: 7-107695815-AAG-A
• MyVariant Identifiers: chr7:g.107336261_107336262del (hg19) ; chr7:g.107695816_107695817del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695817_107695818del , CM000669.2:g.107695817_107695818del	GRCh38
NC_000007.13:g.107336262_107336263del , CM000669.1:g.107336262_107336263del	GRCh37
NC_000007.12:g.107123498_107123499del	NCBI36
NG_008489.1:g.40183_40184del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-116_1438-115del MANE Select	ENSP00000494017.1:n.1438-116_1438-115del
ENST00000644846.1:c.149-116_149-115del
ENST00000265715.7:c.1438-116_1438-115del	ENSP00000265715.3:n.1438-116_1438-115del
ENST00000460748.1:n.541-116_541-115del
ENST00000477350.5:n.285-116_285-115del
ENST00000480841.5:n.287-116_287-115del
ENST00000497446.5:n.453-116_453-115del
NM_000441.1:c.1438-116_1438-115del	NP_000432.1:n.1438-116_1438-115del
XM_005250425.1:c.1438-116_1438-115del	XP_005250482.1:n.1438-116_1438-115del
XM_005250425.2:c.1438-116_1438-115del	XP_005250482.1:n.1438-116_1438-115del
XM_017012318.1:c.1360-116_1360-115del	XP_016867807.1:n.1360-116_1360-115del
NM_000441.2:c.1438-116_1438-115del MANE Select	NP_000432.1:n.1438-116_1438-115del