Canonical Allele Identifier: CA2578988640

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675201_107675203del , CM000669.2:g.107675201_107675203del	GRCh38
NC_000007.13:g.107315646_107315648del , CM000669.1:g.107315646_107315648del	GRCh37
NC_000007.12:g.107102882_107102884del	NCBI36
NG_008489.1:g.19567_19569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+92_765+94del MANE Select	ENSP00000494017.1:n.765+92_765+94del
ENST00000265715.7:c.765+92_765+94del	ENSP00000265715.3:n.765+92_765+94del
NM_000441.1:c.765+92_765+94del	NP_000432.1:n.765+92_765+94del
XM_005250425.1:c.765+92_765+94del	XP_005250482.1:n.765+92_765+94del
XM_006716025.2:c.765+92_765+94del	XP_006716088.1:n.765+92_765+94del
XM_005250425.2:c.765+92_765+94del	XP_005250482.1:n.765+92_765+94del
XM_006716025.3:c.765+92_765+94del	XP_006716088.1:n.765+92_765+94del
XM_017012318.1:c.765+92_765+94del	XP_016867807.1:n.765+92_765+94del
NM_000441.2:c.765+92_765+94del MANE Select	NP_000432.1:n.765+92_765+94del