Canonical Allele Identifier: CA1732750965

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107709868_107709869delinsGC , CM000669.2:g.107709868_107709869delinsGC	GRCh38
NC_000007.13:g.107350313_107350314delinsGC , CM000669.1:g.107350313_107350314delinsGC	GRCh37
NC_000007.12:g.107137549_107137550delinsGC	NCBI36
NG_008489.1:g.54234_54235delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.2090-186_2090-185delinsGC MANE Select	ENSP00000494017.1:n.2090-186_2090-185delinsGC
ENST00000644846.1:c.746-186_746-185delinsGC
ENST00000265715.7:c.2090-186_2090-185delinsGC	ENSP00000265715.3:n.2090-186_2090-185delinsGC
ENST00000492030.2:n.377-287_377-286delinsGC
NM_000441.1:c.2090-186_2090-185delinsGC	NP_000432.1:n.2090-186_2090-185delinsGC
XM_005250425.1:c.2090-186_2090-185delinsGC	XP_005250482.1:n.2090-186_2090-185delinsGC
XM_005250425.2:c.2090-186_2090-185delinsGC	XP_005250482.1:n.2090-186_2090-185delinsGC
XM_017012318.1:c.2012-186_2012-185delinsGC	XP_016867807.1:n.2012-186_2012-185delinsGC
NM_000441.2:c.2090-186_2090-185delinsGC MANE Select	NP_000432.1:n.2090-186_2090-185delinsGC