Canonical Allele Identifier: CA2739278917

Gene: SLC26A4

Linked Data

• ClinVar Variation Id: 2841321
• ClinVar RCV Id: RCV003718937

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701820del , CM000669.2:g.107701820del	GRCh38
NC_000007.13:g.107342265del , CM000669.1:g.107342265del	GRCh37
NC_000007.12:g.107129501del	NCBI36
NG_008489.1:g.46186del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1804-7del MANE Select	ENSP00000494017.1:n.1804-7del
ENST00000644846.1:c.515-7del
ENST00000265715.7:c.1804-7del	ENSP00000265715.3:n.1804-7del
ENST00000480841.5:n.653-7del
ENST00000492030.2:n.91-7del
NM_000441.1:c.1804-7del	NP_000432.1:n.1804-7del
XM_005250425.1:c.1804-7del	XP_005250482.1:n.1804-7del
XM_005250425.2:c.1804-7del	XP_005250482.1:n.1804-7del
XM_017012318.1:c.1726-7del	XP_016867807.1:n.1726-7del
NM_000441.2:c.1804-7del MANE Select	NP_000432.1:n.1804-7del