Canonical Allele Identifier: CA2684467838

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107696045-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696047del , CM000669.2:g.107696047del	GRCh38
NC_000007.13:g.107336492del , CM000669.1:g.107336492del	GRCh37
NC_000007.12:g.107123728del	NCBI36
NG_008489.1:g.40413del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1544+8del MANE Select	ENSP00000494017.1:n.1544+8del
ENST00000644846.1:c.255+8del
ENST00000265715.7:c.1544+8del	ENSP00000265715.3:n.1544+8del
ENST00000477350.5:n.391+8del
ENST00000480841.5:n.393+8del
NM_000441.1:c.1544+8del	NP_000432.1:n.1544+8del
XM_005250425.1:c.1544+8del	XP_005250482.1:n.1544+8del
XM_005250425.2:c.1544+8del	XP_005250482.1:n.1544+8del
XM_017012318.1:c.1466+8del	XP_016867807.1:n.1466+8del
NM_000441.2:c.1544+8del MANE Select	NP_000432.1:n.1544+8del