Canonical Allele Identifier: CA651805642
Gene: SLC26A4 HGNC NCBI

Linked Data

COSMIC: COSN22461776 COSN24071188
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715978_107715979insC , CM000669.2:g.107715978_107715979insC GRCh38
NC_000007.13:g.107356423_107356424insC , CM000669.1:g.107356423_107356424insC GRCh37
NC_000007.12:g.107143659_107143660insC NCBI36
NG_008489.1:g.60344_60345insC

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*532_*533insC MANE Select ENSP00000494017.1:n.*532_*533insC
ENST00000644846.1:c.1531_1532insC
ENST00000265715.7:c.*532_*533insC ENSP00000265715.3:n.*532_*533insC
NM_000441.1:c.*532_*533insC NP_000432.1:n.*532_*533insC
XM_005250425.2:c.*532_*533insC XP_005250482.1:n.*532_*533insC
XM_017012318.1:c.*532_*533insC XP_016867807.1:n.*532_*533insC
NM_000441.2:c.*532_*533insC MANE Select NP_000432.1:n.*532_*533insC
Search 100 bp 5'
Search 100 bp 3'