Canonical Allele Identifier: CA913111813

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107336364_107336365del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695919_107695920del , CM000669.2:g.107695919_107695920del	GRCh38
NC_000007.13:g.107336364_107336365del , CM000669.1:g.107336364_107336365del	GRCh37
NC_000007.12:g.107123600_107123601del	NCBI36
NG_008489.1:g.40285_40286del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-14_1438-13del MANE Select	ENSP00000494017.1:n.1438-14_1438-13del
ENST00000644846.1:c.149-14_149-13del
ENST00000265715.7:c.1438-14_1438-13del	ENSP00000265715.3:n.1438-14_1438-13del
ENST00000460748.1:n.541-14_541-13del
ENST00000477350.5:n.285-14_285-13del
ENST00000480841.5:n.287-14_287-13del
ENST00000497446.5:n.453-14_453-13del
NM_000441.1:c.1438-14_1438-13del	NP_000432.1:n.1438-14_1438-13del
XM_005250425.1:c.1438-14_1438-13del	XP_005250482.1:n.1438-14_1438-13del
XM_005250425.2:c.1438-14_1438-13del	XP_005250482.1:n.1438-14_1438-13del
XM_017012318.1:c.1360-14_1360-13del	XP_016867807.1:n.1360-14_1360-13del
NM_000441.2:c.1438-14_1438-13del MANE Select	NP_000432.1:n.1438-14_1438-13del