Canonical Allele Identifier: CA1732756972
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717320C= , CM000669.2:g.107717320C= GRCh38
NC_000007.13:g.107357765C= , CM000669.1:g.107357765C= GRCh37
NC_000007.12:g.107145001C= NCBI36
NG_008489.1:g.61686C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1874C= MANE Select ENSP00000494017.1:n.*1874C=
ENST00000644846.1:c.2873C=
ENST00000265715.7:c.*1874C= ENSP00000265715.3:n.*1874C=
NM_000441.1:c.*1874C= NP_000432.1:n.*1874C=
NM_000441.2:c.*1874C= MANE Select NP_000432.1:n.*1874C=
Search 100 bp 5'
Search 100 bp 3'