Canonical Allele Identifier: CA457095693
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107336380T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695935T>C , CM000669.2:g.107695935T>C GRCh38
NC_000007.13:g.107336380T>C , CM000669.1:g.107336380T>C GRCh37
NC_000007.12:g.107123616T>C NCBI36
NG_008489.1:g.40301T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1440T>C MANE Select ENSP00000494017.1:p.Val480=
ENST00000644846.1:n.151T>C
ENST00000265715.7:c.1440T>C ENSP00000265715.3:p.Val480=
ENST00000460748.1:n.543T>C
ENST00000477350.5:n.287T>C
ENST00000480841.5:n.289T>C
ENST00000497446.5:n.455T>C
NM_000441.1:c.1440T>C NP_000432.1:p.Val480=
XM_005250425.1:c.1440T>C XP_005250482.1:p.Val480=
XM_005250425.2:c.1440T>C XP_005250482.1:p.Val480=
XM_017012318.1:c.1362T>C XP_016867807.1:p.Val454=
NM_000441.2:c.1440T>C MANE Select NP_000432.1:p.Val480=