Canonical Allele Identifier: CA2578989094

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696065del , CM000669.2:g.107696065del	GRCh38
NC_000007.13:g.107336510del , CM000669.1:g.107336510del	GRCh37
NC_000007.12:g.107123746del	NCBI36
NG_008489.1:g.40431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1544+26del MANE Select	ENSP00000494017.1:n.1544+26del
ENST00000644846.1:c.255+26del
ENST00000265715.7:c.1544+26del	ENSP00000265715.3:n.1544+26del
ENST00000477350.5:n.391+26del
ENST00000480841.5:n.393+26del
NM_000441.1:c.1544+26del	NP_000432.1:n.1544+26del
XM_005250425.1:c.1544+26del	XP_005250482.1:n.1544+26del
XM_005250425.2:c.1544+26del	XP_005250482.1:n.1544+26del
XM_017012318.1:c.1466+26del	XP_016867807.1:n.1466+26del
NM_000441.2:c.1544+26del MANE Select	NP_000432.1:n.1544+26del