Canonical Allele Identifier: CA1732727453

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1790564522

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661815_107661816insAC , CM000669.2:g.107661815_107661816insAC	GRCh38
NC_000007.13:g.107302260_107302261insAC , CM000669.1:g.107302260_107302261insAC	GRCh37
NC_000007.12:g.107089496_107089497insAC	NCBI36
NG_008489.1:g.6181_6182insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+10_164+11insAC MANE Select	ENSP00000494017.1:n.164+10_164+11insAC
ENST00000265715.7:c.164+10_164+11insAC	ENSP00000265715.3:n.164+10_164+11insAC
ENST00000440056.1:c.164+10_164+11insAC	ENSP00000394760.1:n.164+10_164+11insAC
NM_000441.1:c.164+10_164+11insAC	NP_000432.1:n.164+10_164+11insAC
XM_005250425.1:c.164+10_164+11insAC	XP_005250482.1:n.164+10_164+11insAC
XM_006716025.2:c.164+10_164+11insAC	XP_006716088.1:n.164+10_164+11insAC
XM_005250425.2:c.164+10_164+11insAC	XP_005250482.1:n.164+10_164+11insAC
XM_006716025.3:c.164+10_164+11insAC	XP_006716088.1:n.164+10_164+11insAC
XM_017012318.1:c.164+10_164+11insAC	XP_016867807.1:n.164+10_164+11insAC
NM_000441.2:c.164+10_164+11insAC MANE Select	NP_000432.1:n.164+10_164+11insAC