Canonical Allele Identifier: CA2684466558

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107690297-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690299_107690301dup , CM000669.2:g.107690299_107690301dup	GRCh38
NC_000007.13:g.107330744_107330746dup , CM000669.1:g.107330744_107330746dup	GRCh37
NC_000007.12:g.107117980_107117982dup	NCBI36
NG_008489.1:g.34665_34667dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1263+62_1263+64dup MANE Select	ENSP00000494017.1:n.1263+62_1263+64dup
ENST00000265715.7:c.1263+62_1263+64dup	ENSP00000265715.3:n.1263+62_1263+64dup
NM_000441.1:c.1263+62_1263+64dup	NP_000432.1:n.1263+62_1263+64dup
XM_005250425.1:c.1263+62_1263+64dup	XP_005250482.1:n.1263+62_1263+64dup
XM_006716025.2:c.1263+62_1263+64dup	XP_006716088.1:n.1263+62_1263+64dup
XM_005250425.2:c.1263+62_1263+64dup	XP_005250482.1:n.1263+62_1263+64dup
XM_006716025.3:c.1263+62_1263+64dup	XP_006716088.1:n.1263+62_1263+64dup
XM_017012318.1:c.1263+62_1263+64dup	XP_016867807.1:n.1263+62_1263+64dup
NM_000441.2:c.1263+62_1263+64dup MANE Select	NP_000432.1:n.1263+62_1263+64dup