Canonical Allele Identifier: CA2578988913

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701801_107701805del , CM000669.2:g.107701801_107701805del	GRCh38
NC_000007.13:g.107342246_107342250del , CM000669.1:g.107342246_107342250del	GRCh37
NC_000007.12:g.107129482_107129486del	NCBI36
NG_008489.1:g.46167_46171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1804-26_1804-22del MANE Select	ENSP00000494017.1:n.1804-26_1804-22del
ENST00000644846.1:c.515-26_515-22del
ENST00000265715.7:c.1804-26_1804-22del	ENSP00000265715.3:n.1804-26_1804-22del
ENST00000480841.5:n.653-26_653-22del
ENST00000492030.2:n.91-26_91-22del
NM_000441.1:c.1804-26_1804-22del	NP_000432.1:n.1804-26_1804-22del
XM_005250425.1:c.1804-26_1804-22del	XP_005250482.1:n.1804-26_1804-22del
XM_005250425.2:c.1804-26_1804-22del	XP_005250482.1:n.1804-26_1804-22del
XM_017012318.1:c.1726-26_1726-22del	XP_016867807.1:n.1726-26_1726-22del
NM_000441.2:c.1804-26_1804-22del MANE Select	NP_000432.1:n.1804-26_1804-22del