Canonical Allele Identifier: CA457098532

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1438508849
• MyVariant Identifiers: chr7:g.107338541C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107698096C>G , CM000669.2:g.107698096C>G	GRCh38
NC_000007.13:g.107338541C>G , CM000669.1:g.107338541C>G	GRCh37
NC_000007.12:g.107125777C>G	NCBI36
NG_008489.1:g.42462C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1599C>G MANE Select	ENSP00000494017.1:p.Thr533=
ENST00000644846.1:c.310C>G
ENST00000265715.7:c.1599C>G	ENSP00000265715.3:p.Thr533=
ENST00000477350.5:n.446C>G
ENST00000480841.5:n.448C>G
NM_000441.1:c.1599C>G	NP_000432.1:p.Thr533=
XM_005250425.1:c.1599C>G	XP_005250482.1:p.Thr533=
XM_005250425.2:c.1599C>G	XP_005250482.1:p.Thr533=
XM_017012318.1:c.1521C>G	XP_016867807.1:p.Thr507=
NM_000441.2:c.1599C>G MANE Select	NP_000432.1:p.Thr533=