Canonical Allele Identifier: CA1732752765

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695698A= , CM000669.2:g.107695698A=	GRCh38
NC_000007.13:g.107336143A= , CM000669.1:g.107336143A=	GRCh37
NC_000007.12:g.107123379A=	NCBI36
NG_008489.1:g.40064A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-235A= MANE Select	ENSP00000494017.1:n.1438-235A=
ENST00000644846.1:c.149-235A=
ENST00000265715.7:c.1438-235A=	ENSP00000265715.3:n.1438-235A=
ENST00000460748.1:n.541-235A=
ENST00000477350.5:n.285-235A=
ENST00000480841.5:n.287-235A=
ENST00000497446.5:n.453-235A=
NM_000441.1:c.1438-235A=	NP_000432.1:n.1438-235A=
XM_005250425.1:c.1438-235A=	XP_005250482.1:n.1438-235A=
XM_005250425.2:c.1438-235A=	XP_005250482.1:n.1438-235A=
XM_017012318.1:c.1360-235A=	XP_016867807.1:n.1360-235A=
NM_000441.2:c.1438-235A= MANE Select	NP_000432.1:n.1438-235A=