Canonical Allele Identifier: CA1732751247

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694262C= , CM000669.2:g.107694262C=	GRCh38
NC_000007.13:g.107334707C= , CM000669.1:g.107334707C=	GRCh37
NC_000007.12:g.107121943C=	NCBI36
NG_008489.1:g.38628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1264-141C= MANE Select	ENSP00000494017.1:n.1264-141C=
ENST00000265715.7:c.1264-141C=	ENSP00000265715.3:n.1264-141C=
ENST00000460748.1:n.367-141C=
ENST00000477350.5:n.189-359C=
ENST00000480841.5:n.113-141C=
ENST00000497446.5:n.279-141C=
NM_000441.1:c.1264-141C=	NP_000432.1:n.1264-141C=
XM_005250425.1:c.1264-141C=	XP_005250482.1:n.1264-141C=
XM_006716025.2:c.*702C=	XP_006716088.1:n.*702C=
XM_005250425.2:c.1264-141C=	XP_005250482.1:n.1264-141C=
XM_006716025.3:c.*702C=	XP_006716088.1:n.*702C=
XM_017012318.1:c.1264-359C=	XP_016867807.1:n.1264-359C=
NM_000441.2:c.1264-141C= MANE Select	NP_000432.1:n.1264-141C=