Canonical Allele Identifier: CA2684466564

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107690304-T-TCGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690306_107690309dup , CM000669.2:g.107690306_107690309dup	GRCh38
NC_000007.13:g.107330751_107330754dup , CM000669.1:g.107330751_107330754dup	GRCh37
NC_000007.12:g.107117987_107117990dup	NCBI36
NG_008489.1:g.34672_34675dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1263+69_1263+72dup MANE Select	ENSP00000494017.1:n.1263+69_1263+72dup
ENST00000265715.7:c.1263+69_1263+72dup	ENSP00000265715.3:n.1263+69_1263+72dup
NM_000441.1:c.1263+69_1263+72dup	NP_000432.1:n.1263+69_1263+72dup
XM_005250425.1:c.1263+69_1263+72dup	XP_005250482.1:n.1263+69_1263+72dup
XM_006716025.2:c.1263+69_1263+72dup	XP_006716088.1:n.1263+69_1263+72dup
XM_005250425.2:c.1263+69_1263+72dup	XP_005250482.1:n.1263+69_1263+72dup
XM_006716025.3:c.1263+69_1263+72dup	XP_006716088.1:n.1263+69_1263+72dup
XM_017012318.1:c.1263+69_1263+72dup	XP_016867807.1:n.1263+69_1263+72dup
NM_000441.2:c.1263+69_1263+72dup MANE Select	NP_000432.1:n.1263+69_1263+72dup