Canonical Allele Identifier: CA2684463366

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107675196-T-TGGCTCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107675197_107675203dup , CM000669.2:g.107675197_107675203dup	GRCh38
NC_000007.13:g.107315642_107315648dup , CM000669.1:g.107315642_107315648dup	GRCh37
NC_000007.12:g.107102878_107102884dup	NCBI36
NG_008489.1:g.19563_19569dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.765+88_765+94dup MANE Select	ENSP00000494017.1:n.765+88_765+94dup
ENST00000265715.7:c.765+88_765+94dup	ENSP00000265715.3:n.765+88_765+94dup
NM_000441.1:c.765+88_765+94dup	NP_000432.1:n.765+88_765+94dup
XM_005250425.1:c.765+88_765+94dup	XP_005250482.1:n.765+88_765+94dup
XM_006716025.2:c.765+88_765+94dup	XP_006716088.1:n.765+88_765+94dup
XM_005250425.2:c.765+88_765+94dup	XP_005250482.1:n.765+88_765+94dup
XM_006716025.3:c.765+88_765+94dup	XP_006716088.1:n.765+88_765+94dup
XM_017012318.1:c.765+88_765+94dup	XP_016867807.1:n.765+88_765+94dup
NM_000441.2:c.765+88_765+94dup MANE Select	NP_000432.1:n.765+88_765+94dup