Canonical Allele Identifier: CA2684465304

Gene: SLC26A4 SLC26A4-AS1

Linked Data

• gnomAD v4: 7-107661409-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661409G>A , CM000669.2:g.107661409G>A	GRCh38
NC_000007.13:g.107301854G>A , CM000669.1:g.107301854G>A	GRCh37
NC_000007.12:g.107089090G>A	NCBI36
NG_008489.1:g.5775G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.-3-230G>A (SLC26A4) MANE Select	ENSP00000494017.1:n.-3-230G>A
ENST00000265715.7:c.-3-230G>A (SLC26A4)	ENSP00000265715.3:n.-3-230G>A
ENST00000440056.1:c.-4+202G>A (SLC26A4)	ENSP00000394760.1:n.-4+202G>A
NM_000441.1:c.-3-230G>A (SLC26A4)	NP_000432.1:n.-3-230G>A
NR_028137.1:n.197+193C>T (SLC26A4-AS1)
XM_005250425.1:c.-4+202G>A (SLC26A4)	XP_005250482.1:n.-4+202G>A
XM_005250425.2:c.-4+202G>A (SLC26A4)	XP_005250482.1:n.-4+202G>A
NM_000441.2:c.-3-230G>A (SLC26A4) MANE Select	NP_000432.1:n.-3-230G>A