Canonical Allele Identifier: CA2684457568

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107662010-C-CGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662012_107662013insTGA , CM000669.2:g.107662012_107662013insTGA	GRCh38
NC_000007.13:g.107302457_107302458insTGA , CM000669.1:g.107302457_107302458insTGA	GRCh37
NC_000007.12:g.107089693_107089694insTGA	NCBI36
NG_008489.1:g.6378_6379insTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+207_164+208insTGA MANE Select	ENSP00000494017.1:n.164+207_164+208insTGA
ENST00000265715.7:c.164+207_164+208insTGA	ENSP00000265715.3:n.164+207_164+208insTGA
ENST00000440056.1:c.164+207_164+208insTGA	ENSP00000394760.1:n.164+207_164+208insTGA
NM_000441.1:c.164+207_164+208insTGA	NP_000432.1:n.164+207_164+208insTGA
XM_005250425.1:c.164+207_164+208insTGA	XP_005250482.1:n.164+207_164+208insTGA
XM_006716025.2:c.164+207_164+208insTGA	XP_006716088.1:n.164+207_164+208insTGA
XM_005250425.2:c.164+207_164+208insTGA	XP_005250482.1:n.164+207_164+208insTGA
XM_006716025.3:c.164+207_164+208insTGA	XP_006716088.1:n.164+207_164+208insTGA
XM_017012318.1:c.164+207_164+208insTGA	XP_016867807.1:n.164+207_164+208insTGA
NM_000441.2:c.164+207_164+208insTGA MANE Select	NP_000432.1:n.164+207_164+208insTGA