Canonical Allele Identifier: CA1732727748

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662025_107662026delinsTG , CM000669.2:g.107662025_107662026delinsTG	GRCh38
NC_000007.13:g.107302470_107302471delinsTG , CM000669.1:g.107302470_107302471delinsTG	GRCh37
NC_000007.12:g.107089706_107089707delinsTG	NCBI36
NG_008489.1:g.6391_6392delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+220_164+221delinsTG MANE Select	ENSP00000494017.1:n.164+220_164+221delinsTG
ENST00000265715.7:c.164+220_164+221delinsTG	ENSP00000265715.3:n.164+220_164+221delinsTG
ENST00000440056.1:c.164+220_164+221delinsTG	ENSP00000394760.1:n.164+220_164+221delinsTG
NM_000441.1:c.164+220_164+221delinsTG	NP_000432.1:n.164+220_164+221delinsTG
XM_005250425.1:c.164+220_164+221delinsTG	XP_005250482.1:n.164+220_164+221delinsTG
XM_006716025.2:c.164+220_164+221delinsTG	XP_006716088.1:n.164+220_164+221delinsTG
XM_005250425.2:c.164+220_164+221delinsTG	XP_005250482.1:n.164+220_164+221delinsTG
XM_006716025.3:c.164+220_164+221delinsTG	XP_006716088.1:n.164+220_164+221delinsTG
XM_017012318.1:c.164+220_164+221delinsTG	XP_016867807.1:n.164+220_164+221delinsTG
NM_000441.2:c.164+220_164+221delinsTG MANE Select	NP_000432.1:n.164+220_164+221delinsTG