Canonical Allele Identifier: CA457104013
Gene: SLC26A4 HGNC NCBI
SLC26A4-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107302057C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661612C>G , CM000669.2:g.107661612C>G GRCh38
NC_000007.13:g.107302057C>G , CM000669.1:g.107302057C>G GRCh37
NC_000007.12:g.107089293C>G NCBI36
NG_008489.1:g.5978C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.-3-27C>G (SLC26A4) MANE Select ENSP00000494017.1:n.-3-27C>G
ENST00000265715.7:c.-3-27C>G (SLC26A4) ENSP00000265715.3:n.-3-27C>G
ENST00000440056.1:c.-3-27C>G (SLC26A4) ENSP00000394760.1:n.-3-27C>G
NM_000441.1:c.-3-27C>G (SLC26A4) NP_000432.1:n.-3-27C>G
NR_028137.1:n.187G>C (SLC26A4-AS1)
XM_005250425.1:c.-3-27C>G (SLC26A4) XP_005250482.1:n.-3-27C>G
XM_005250425.2:c.-3-27C>G (SLC26A4) XP_005250482.1:n.-3-27C>G
NM_000441.2:c.-3-27C>G (SLC26A4) MANE Select NP_000432.1:n.-3-27C>G