Canonical Allele Identifier: CA1732745767

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107674086_107674087delinsAT , CM000669.2:g.107674086_107674087delinsAT	GRCh38
NC_000007.13:g.107314531_107314532delinsAT , CM000669.1:g.107314531_107314532delinsAT	GRCh37
NC_000007.12:g.107101767_107101768delinsAT	NCBI36
NG_008489.1:g.18452_18453delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.416-78_416-77delinsAT MANE Select	ENSP00000494017.1:n.416-78_416-77delinsAT
ENST00000265715.7:c.416-78_416-77delinsAT	ENSP00000265715.3:n.416-78_416-77delinsAT
NM_000441.1:c.416-78_416-77delinsAT	NP_000432.1:n.416-78_416-77delinsAT
XM_005250425.1:c.416-78_416-77delinsAT	XP_005250482.1:n.416-78_416-77delinsAT
XM_006716025.2:c.416-78_416-77delinsAT	XP_006716088.1:n.416-78_416-77delinsAT
XM_005250425.2:c.416-78_416-77delinsAT	XP_005250482.1:n.416-78_416-77delinsAT
XM_006716025.3:c.416-78_416-77delinsAT	XP_006716088.1:n.416-78_416-77delinsAT
XM_017012318.1:c.416-78_416-77delinsAT	XP_016867807.1:n.416-78_416-77delinsAT
NM_000441.2:c.416-78_416-77delinsAT MANE Select	NP_000432.1:n.416-78_416-77delinsAT