Canonical Allele Identifier: CA1732752958

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695844G= , CM000669.2:g.107695844G=	GRCh38
NC_000007.13:g.107336289G= , CM000669.1:g.107336289G=	GRCh37
NC_000007.12:g.107123525G=	NCBI36
NG_008489.1:g.40210G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-89G= MANE Select	ENSP00000494017.1:n.1438-89G=
ENST00000644846.1:c.149-89G=
ENST00000265715.7:c.1438-89G=	ENSP00000265715.3:n.1438-89G=
ENST00000460748.1:n.541-89G=
ENST00000477350.5:n.285-89G=
ENST00000480841.5:n.287-89G=
ENST00000497446.5:n.453-89G=
NM_000441.1:c.1438-89G=	NP_000432.1:n.1438-89G=
XM_005250425.1:c.1438-89G=	XP_005250482.1:n.1438-89G=
XM_005250425.2:c.1438-89G=	XP_005250482.1:n.1438-89G=
XM_017012318.1:c.1360-89G=	XP_016867807.1:n.1360-89G=
NM_000441.2:c.1438-89G= MANE Select	NP_000432.1:n.1438-89G=