Canonical Allele Identifier: CA2578988731
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683534_107683544del , CM000669.2:g.107683534_107683544del GRCh38
NC_000007.13:g.107323979_107323989del , CM000669.1:g.107323979_107323989del GRCh37
NC_000007.12:g.107111215_107111225del NCBI36
NG_008489.1:g.27900_27910del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.998_1001+7del
ENST00000265715.7:c.998_1001+7del
NM_000441.1:c.998_1001+7del
XM_005250425.1:c.998_1001+7del
XM_006716025.2:c.998_1001+7del
XM_005250425.2:c.998_1001+7del
XM_006716025.3:c.998_1001+7del
XM_017012318.1:c.998_1001+7del
NM_000441.2:c.998_1001+7del