Canonical Allele Identifier: CA1732751177
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710061G= , CM000669.2:g.107710061G= GRCh38
NC_000007.13:g.107350506G= , CM000669.1:g.107350506G= GRCh37
NC_000007.12:g.107137742G= NCBI36
NG_008489.1:g.54427G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2097G= MANE Select ENSP00000494017.1:p.Val699=
ENST00000644846.1:c.753G=
ENST00000265715.7:c.2097G= ENSP00000265715.3:p.Val699=
ENST00000492030.2:n.377-94G=
NM_000441.1:c.2097G= NP_000432.1:p.Val699=
XM_005250425.1:c.2097G= XP_005250482.1:p.Val699=
XM_005250425.2:c.2097G= XP_005250482.1:p.Val699=
XM_017012318.1:c.2019G= XP_016867807.1:p.Val673=
NM_000441.2:c.2097G= MANE Select NP_000432.1:p.Val699=