Canonical Allele Identifier: CA457104567
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107350518G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710073G>A , CM000669.2:g.107710073G>A GRCh38
NC_000007.13:g.107350518G>A , CM000669.1:g.107350518G>A GRCh37
NC_000007.12:g.107137754G>A NCBI36
NG_008489.1:g.54439G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2109G>A MANE Select ENSP00000494017.1:p.Leu703=
ENST00000644846.1:c.765G>A
ENST00000265715.7:c.2109G>A ENSP00000265715.3:p.Leu703=
ENST00000492030.2:n.377-82G>A
NM_000441.1:c.2109G>A NP_000432.1:p.Leu703=
XM_005250425.1:c.2109G>A XP_005250482.1:p.Leu703=
XM_005250425.2:c.2109G>A XP_005250482.1:p.Leu703=
XM_017012318.1:c.2031G>A XP_016867807.1:p.Leu677=
NM_000441.2:c.2109G>A MANE Select NP_000432.1:p.Leu703=