Canonical Allele Identifier: CA1732727787

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662066_107662068delinsGTC , CM000669.2:g.107662066_107662068delinsGTC	GRCh38
NC_000007.13:g.107302511_107302513delinsGTC , CM000669.1:g.107302511_107302513delinsGTC	GRCh37
NC_000007.12:g.107089747_107089749delinsGTC	NCBI36
NG_008489.1:g.6432_6434delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+261_164+263delinsGTC MANE Select	ENSP00000494017.1:n.164+261_164+263delinsGTC
ENST00000265715.7:c.164+261_164+263delinsGTC	ENSP00000265715.3:n.164+261_164+263delinsGTC
ENST00000440056.1:c.164+261_164+263delinsGTC	ENSP00000394760.1:n.164+261_164+263delinsGTC
NM_000441.1:c.164+261_164+263delinsGTC	NP_000432.1:n.164+261_164+263delinsGTC
XM_005250425.1:c.164+261_164+263delinsGTC	XP_005250482.1:n.164+261_164+263delinsGTC
XM_006716025.2:c.164+261_164+263delinsGTC	XP_006716088.1:n.164+261_164+263delinsGTC
XM_005250425.2:c.164+261_164+263delinsGTC	XP_005250482.1:n.164+261_164+263delinsGTC
XM_006716025.3:c.164+261_164+263delinsGTC	XP_006716088.1:n.164+261_164+263delinsGTC
XM_017012318.1:c.164+261_164+263delinsGTC	XP_016867807.1:n.164+261_164+263delinsGTC
NM_000441.2:c.164+261_164+263delinsGTC MANE Select	NP_000432.1:n.164+261_164+263delinsGTC