Canonical Allele Identifier: CA1732755767

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107715975G= , CM000669.2:g.107715975G=	GRCh38
NC_000007.13:g.107356420G= , CM000669.1:g.107356420G=	GRCh37
NC_000007.12:g.107143656G=	NCBI36
NG_008489.1:g.60341G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.*529G= MANE Select	ENSP00000494017.1:n.*529G=
ENST00000644846.1:c.1528G=
ENST00000265715.7:c.*529G=	ENSP00000265715.3:n.*529G=
NM_000441.1:c.*529G=	NP_000432.1:n.*529G=
XM_005250425.2:c.*529G=	XP_005250482.1:n.*529G=
XM_017012318.1:c.*529G=	XP_016867807.1:n.*529G=
NM_000441.2:c.*529G= MANE Select	NP_000432.1:n.*529G=