Canonical Allele Identifier: CA2684465530
Gene: SLC26A4 HGNC NCBI
SLC26A4-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-107661508-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661508A>C , CM000669.2:g.107661508A>C GRCh38
NC_000007.13:g.107301953A>C , CM000669.1:g.107301953A>C GRCh37
NC_000007.12:g.107089189A>C NCBI36
NG_008489.1:g.5874A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.-3-131A>C (SLC26A4) MANE Select ENSP00000494017.1:n.-3-131A>C
ENST00000265715.7:c.-3-131A>C (SLC26A4) ENSP00000265715.3:n.-3-131A>C
ENST00000440056.1:c.-3-131A>C (SLC26A4) ENSP00000394760.1:n.-3-131A>C
NM_000441.1:c.-3-131A>C (SLC26A4) NP_000432.1:n.-3-131A>C
NR_028137.1:n.197+94T>G (SLC26A4-AS1)
XM_005250425.1:c.-3-131A>C (SLC26A4) XP_005250482.1:n.-3-131A>C
XM_005250425.2:c.-3-131A>C (SLC26A4) XP_005250482.1:n.-3-131A>C
NM_000441.2:c.-3-131A>C (SLC26A4) MANE Select NP_000432.1:n.-3-131A>C
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