Canonical Allele Identifier: CA1732759062
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701804T= , CM000669.2:g.107701804T= GRCh38
NC_000007.13:g.107342249T= , CM000669.1:g.107342249T= GRCh37
NC_000007.12:g.107129485T= NCBI36
NG_008489.1:g.46170T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-23T= MANE Select ENSP00000494017.1:n.1804-23T=
ENST00000644846.1:c.515-23T=
ENST00000265715.7:c.1804-23T= ENSP00000265715.3:n.1804-23T=
ENST00000480841.5:n.653-23T=
ENST00000492030.2:n.91-23T=
NM_000441.1:c.1804-23T= NP_000432.1:n.1804-23T=
XM_005250425.1:c.1804-23T= XP_005250482.1:n.1804-23T=
XM_005250425.2:c.1804-23T= XP_005250482.1:n.1804-23T=
XM_017012318.1:c.1726-23T= XP_016867807.1:n.1726-23T=
NM_000441.2:c.1804-23T= MANE Select NP_000432.1:n.1804-23T=