Canonical Allele Identifier: CA2578989117

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107697957del , CM000669.2:g.107697957del	GRCh38
NC_000007.13:g.107338402del , CM000669.1:g.107338402del	GRCh37
NC_000007.12:g.107125638del	NCBI36
NG_008489.1:g.42323del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1545-85del MANE Select	ENSP00000494017.1:n.1545-85del
ENST00000644846.1:c.256-85del
ENST00000265715.7:c.1545-85del	ENSP00000265715.3:n.1545-85del
ENST00000477350.5:n.392-85del
ENST00000480841.5:n.394-85del
NM_000441.1:c.1545-85del	NP_000432.1:n.1545-85del
XM_005250425.1:c.1545-85del	XP_005250482.1:n.1545-85del
XM_005250425.2:c.1545-85del	XP_005250482.1:n.1545-85del
XM_017012318.1:c.1467-85del	XP_016867807.1:n.1467-85del
NM_000441.2:c.1545-85del MANE Select	NP_000432.1:n.1545-85del