Canonical Allele Identifier: CA1732726796

Gene: SLC26A4 SLC26A4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661468_107661471delinsTGGG , CM000669.2:g.107661468_107661471delinsTGGG	GRCh38
NC_000007.13:g.107301913_107301916delinsTGGG , CM000669.1:g.107301913_107301916delinsTGGG	GRCh37
NC_000007.12:g.107089149_107089152delinsTGGG	NCBI36
NG_008489.1:g.5834_5837delinsTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.-3-171_-3-168delinsTGGG (SLC26A4) MANE Select	ENSP00000494017.1:n.-3-171_-3-168delinsTGGG
ENST00000265715.7:c.-3-171_-3-168delinsTGGG (SLC26A4)	ENSP00000265715.3:n.-3-171_-3-168delinsTGGG
ENST00000440056.1:c.-3-171_-3-168delinsTGGG (SLC26A4)	ENSP00000394760.1:n.-3-171_-3-168delinsTGGG
NM_000441.1:c.-3-171_-3-168delinsTGGG (SLC26A4)	NP_000432.1:n.-3-171_-3-168delinsTGGG
NR_028137.1:n.197+131_197+134delinsCCCA (SLC26A4-AS1)
XM_005250425.1:c.-3-171_-3-168delinsTGGG (SLC26A4)	XP_005250482.1:n.-3-171_-3-168delinsTGGG
XM_005250425.2:c.-3-171_-3-168delinsTGGG (SLC26A4)	XP_005250482.1:n.-3-171_-3-168delinsTGGG
NM_000441.2:c.-3-171_-3-168delinsTGGG (SLC26A4) MANE Select	NP_000432.1:n.-3-171_-3-168delinsTGGG