Canonical Allele Identifier: CA2715574470

Gene: SLC26A4

Linked Data

• dbSNP Id: rs2129318224

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701810_107701823del , CM000669.2:g.107701810_107701823del	GRCh38
NC_000007.13:g.107342255_107342268del , CM000669.1:g.107342255_107342268del	GRCh37
NC_000007.12:g.107129491_107129504del	NCBI36
NG_008489.1:g.46176_46189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-17_1804-4del MANE Select	ENSP00000494017.1:n.1804-17_1804-4del
ENST00000644846.1:c.515-17_515-4del
ENST00000265715.7:c.1804-17_1804-4del	ENSP00000265715.3:n.1804-17_1804-4del
ENST00000480841.5:n.653-17_653-4del
ENST00000492030.2:n.91-17_91-4del
NM_000441.1:c.1804-17_1804-4del	NP_000432.1:n.1804-17_1804-4del
XM_005250425.1:c.1804-17_1804-4del	XP_005250482.1:n.1804-17_1804-4del
XM_005250425.2:c.1804-17_1804-4del	XP_005250482.1:n.1804-17_1804-4del
XM_017012318.1:c.1726-17_1726-4del	XP_016867807.1:n.1726-17_1726-4del
NM_000441.2:c.1804-17_1804-4del MANE Select	NP_000432.1:n.1804-17_1804-4del