Canonical Allele Identifier: CA1732742132

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683618A= , CM000669.2:g.107683618A=	GRCh38
NC_000007.13:g.107324063A= , CM000669.1:g.107324063A=	GRCh37
NC_000007.12:g.107111299A=	NCBI36
NG_008489.1:g.27984A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1001+81A= MANE Select	ENSP00000494017.1:n.1001+81A=
ENST00000265715.7:c.1001+81A=	ENSP00000265715.3:n.1001+81A=
NM_000441.1:c.1001+81A=	NP_000432.1:n.1001+81A=
XM_005250425.1:c.1001+81A=	XP_005250482.1:n.1001+81A=
XM_006716025.2:c.1001+81A=	XP_006716088.1:n.1001+81A=
XM_005250425.2:c.1001+81A=	XP_005250482.1:n.1001+81A=
XM_006716025.3:c.1001+81A=	XP_006716088.1:n.1001+81A=
XM_017012318.1:c.1001+81A=	XP_016867807.1:n.1001+81A=
NM_000441.2:c.1001+81A= MANE Select	NP_000432.1:n.1001+81A=