Canonical Allele Identifier: CA1732727038

Gene: SLC26A4 SLC26A4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107661640T= , CM000669.2:g.107661640T=	GRCh38
NC_000007.13:g.107302085T= , CM000669.1:g.107302085T=	GRCh37
NC_000007.12:g.107089321T=	NCBI36
NG_008489.1:g.6006T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.-2T= (SLC26A4) MANE Select	ENSP00000494017.1:n.-2T=
ENST00000265715.7:c.-2T= (SLC26A4)	ENSP00000265715.3:n.-2T=
ENST00000440056.1:c.-2T= (SLC26A4)	ENSP00000394760.1:n.-2T=
NM_000441.1:c.-2T= (SLC26A4)	NP_000432.1:n.-2T=
NR_028137.1:n.159A= (SLC26A4-AS1)
XM_005250425.1:c.-2T= (SLC26A4)	XP_005250482.1:n.-2T=
XM_006716025.2:c.-2T= (SLC26A4)	XP_006716088.1:n.-2T=
XM_005250425.2:c.-2T= (SLC26A4)	XP_005250482.1:n.-2T=
XM_006716025.3:c.-2T= (SLC26A4)	XP_006716088.1:n.-2T=
XM_017012318.1:c.-2T= (SLC26A4)	XP_016867807.1:n.-2T=
NM_000441.2:c.-2T= (SLC26A4) MANE Select	NP_000432.1:n.-2T=