Canonical Allele Identifier: CA4432702
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs771345264
ExAC: 7:107329692 G / GA
gnomAD v2: 7-107329692-G-GA
gnomAD v3: 7-107689247-G-GA
gnomAD v4: 7-107689247-G-GA
MyVariant Identifiers: chr7:g.107329693_107329694insA (hg19) chr7:g.107329692_107329693insA (hg19) chr7:g.107689248_107689249insA (hg38) chr7:g.107689247_107689248insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689254dup , CM000669.2:g.107689254dup GRCh38
NC_000007.13:g.107329699dup , CM000669.1:g.107329699dup GRCh37
NC_000007.12:g.107116935dup NCBI36
NG_008489.1:g.33620dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+54dup MANE Select ENSP00000494017.1:n.1149+54dup
ENST00000265715.7:c.1149+54dup ENSP00000265715.3:n.1149+54dup
NM_000441.1:c.1149+54dup NP_000432.1:n.1149+54dup
XM_005250425.1:c.1149+54dup XP_005250482.1:n.1149+54dup
XM_006716025.2:c.1149+54dup XP_006716088.1:n.1149+54dup
XM_005250425.2:c.1149+54dup XP_005250482.1:n.1149+54dup
XM_006716025.3:c.1149+54dup XP_006716088.1:n.1149+54dup
XM_017012318.1:c.1149+54dup XP_016867807.1:n.1149+54dup
NM_000441.2:c.1149+54dup MANE Select NP_000432.1:n.1149+54dup
Search 100 bp 5'
Search 100 bp 3'