Canonical Allele Identifier: CA2684467797

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107695854-CTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695857_107695859del , CM000669.2:g.107695857_107695859del	GRCh38
NC_000007.13:g.107336302_107336304del , CM000669.1:g.107336302_107336304del	GRCh37
NC_000007.12:g.107123538_107123540del	NCBI36
NG_008489.1:g.40223_40225del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-76_1438-74del MANE Select	ENSP00000494017.1:n.1438-76_1438-74del
ENST00000644846.1:c.149-76_149-74del
ENST00000265715.7:c.1438-76_1438-74del	ENSP00000265715.3:n.1438-76_1438-74del
ENST00000460748.1:n.541-76_541-74del
ENST00000477350.5:n.285-76_285-74del
ENST00000480841.5:n.287-76_287-74del
ENST00000497446.5:n.453-76_453-74del
NM_000441.1:c.1438-76_1438-74del	NP_000432.1:n.1438-76_1438-74del
XM_005250425.1:c.1438-76_1438-74del	XP_005250482.1:n.1438-76_1438-74del
XM_005250425.2:c.1438-76_1438-74del	XP_005250482.1:n.1438-76_1438-74del
XM_017012318.1:c.1360-76_1360-74del	XP_016867807.1:n.1360-76_1360-74del
NM_000441.2:c.1438-76_1438-74del MANE Select	NP_000432.1:n.1438-76_1438-74del