Canonical Allele Identifier: CA2518943388

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107696053-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696053_107696054insC , CM000669.2:g.107696053_107696054insC	GRCh38
NC_000007.13:g.107336498_107336499insC , CM000669.1:g.107336498_107336499insC	GRCh37
NC_000007.12:g.107123734_107123735insC	NCBI36
NG_008489.1:g.40419_40420insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1544+14_1544+15insC MANE Select	ENSP00000494017.1:n.1544+14_1544+15insC
ENST00000644846.1:c.255+14_255+15insC
ENST00000265715.7:c.1544+14_1544+15insC	ENSP00000265715.3:n.1544+14_1544+15insC
ENST00000477350.5:n.391+14_391+15insC
ENST00000480841.5:n.393+14_393+15insC
NM_000441.1:c.1544+14_1544+15insC	NP_000432.1:n.1544+14_1544+15insC
XM_005250425.1:c.1544+14_1544+15insC	XP_005250482.1:n.1544+14_1544+15insC
XM_005250425.2:c.1544+14_1544+15insC	XP_005250482.1:n.1544+14_1544+15insC
XM_017012318.1:c.1466+14_1466+15insC	XP_016867807.1:n.1466+14_1466+15insC
NM_000441.2:c.1544+14_1544+15insC MANE Select	NP_000432.1:n.1544+14_1544+15insC